1. NOTICE OF FILING
      2. THIS FILING IS SUBMITTED ON RECYCLED PAPER
      3. Representing NoveonInc.
      4. Noveon-HenxyPlant Experience:
      5. Noveon-Henry Plant Wastewater Treatment Facilities
      6. Plant
      7. 2.1 Single Stage Nitrification, Powdered Activated Carbon Addition, EffluentIon
      8. Nitrification
      9. 2.8 Full-Scale Trial of Pretreatment and Single StageNitrification
      10. Reduction Processes
      11. 5.0 SUMMARY
      12. CERTIFICATE OF SERVICE
      13. EXHIBIT A
  1. T. Houston Flippin, P.E., DEE
      1. Pulp and Paper
      2. Hazardous Waste
      3. Textiles
      4. Food Processing
      5. Combined Municipal/Industrial Wastewater Management
      6. Municipal Wastewater Management
      7.  
      8. Permitting
      9. Toxicity Reduction
      10. EXHIBIT B
      11. TYPES AND USES OFNITRIFICATION INHIBITORS
      12. WHERE SHOULDNITRIFICATION INHIBITORS BE USED?
      13. ADDITIONAL CONSIDERATIONS WHENUSING NITRIFICATION INHIBITORS
      14. EXHIBIT C
  2. MEMORANDUM
      1. FIGURE 1
      2. BLOCK FLOW DIAGRAM OF WASTESTREAM
      3. ALTERNATIVE NO.2- ALKALINE AIR STRIPPING OF PVC TANK CONTENTS
      4. ALTERNATIVE NO.3- ALKALINE AIR STRIPPING OF SECONDARY CLARIFIER EFFLUENT
      5. FIGURE 2
      6. BLOCK FLOW DIAGRAM OF ALKALINEAIR STRIPPING TREATMENT ALTERNATIVES
      7. FIGURE 3
      8. BLOCK FLOW DIAGRAM OF STRUVITEPRECIPITATION TREATMENT ALTERNATIVE
      9. - (No.4)
      10. FIGURE 4
      11. BLOCK FLOW DIAGRAM OF BREAKPOINTCHLORINATION ALTERNATIVE
      12. FIGURE 5
      13. BLOCK FLOW DIAGRAM OF NON-PC WASTESTREAMNITRIFICATION TREATMENT ALTERNATIVE
      14. FIGURE 6
      15. BLOCK FLOW DIAGRAM OF COMBINED WASTESTREAMNITRIFICATION TREATMENT ALTERNATIVE
      16. (No. 7)
      17. BLOCK FLOW DIAGRAM OF OZONE
      18. FIGURE 9
      19. BLOCK FLOW DIAGRAM OF TERTIARYNITRIFICATION TREATMENT ALTERNATIVE
      20. (No. 10)
      21. Comparison of Costs and Removals of Effluent NH3-N Removal Processes

REC~VED
CLERK’S OFFICE
FEB
6
2OU~l
BEFORE THE ILLINOIS POLLUTION CONTROL BOARD
STATE
OF
ILL(NO~S
Pollution
Control Board
Illinois Enviromnental
)
Protection Agency
)
IN THE MATTER OF:
Petition ofNoveon, Inc.
for an Adjusted Standard from
35
Iii.
Adm. Code 304.122
Dorothy M.
Gunn, Clerk
Illinois Pollution Control Board
James R. Thompson Center
100 West Randolph Street
Suite
11-500
Chicago, IL
60601
Deborah Williams
Assistant Counsel
Division of Legal Counsel
Illinois Environmental Protection
Agency
1021 N. Grand Avenue East
Springfield, IL
62794-9276
BradleyP. Halloran
Hearing Officer
Illinois Pollution Control Board
James R. Thompson Center
100 West Randolph Street
Suite 11-500
Chicago, IL
60601
PLEASE
TAKE
NOTICE
that
on
Friday,
February
6,
2004,
we filed the
Written
Expert Testimony ofHouston Flippin, a copy ofwhich is herewith served upon you.
Richard J. Kissel
Mark Latham
Sheila H. Deely
GARDNER CARTON & DOUGLAS LLP
191
N. Wacker Drive
Suite 3700
Chicago, IL
60606
312-569-1000
Respectfully submitted, NOVEON, INC.
‘-II
By:
~A72
~
One ofIts Attorneys
Noveon, Inc.
V.
)
)
)
)
PCB 91-17
(Permit Appeal)
)
)
)
)
ASO2-5
)
)
)
NOTICE OF FILING
THIS FILING IS SUBMITTED
ON RECYCLED PAPER

RECE
WED
CLERK’S OFFICE
FEB
-
62004
STATE OF ILLINOIS
Pollution Control
Board
Petition ofNoveon, Inc. AS 02-5 For An Adjusted Standard
NPDES Adjusted From 35
ILL
ADM. Code Standard 304.122
Written Testimony of
T. Houston
Flippin
as wastewatertreatment
expert
representing Noveon, Inc. in
this
proceeding.
Introduction
and
Experience ofT. Houston
Flippin
asWastewater Treatment
Expert
Representing NoveonInc.
My
name
is Thomas Houston
Flippin.
I was retained by Noveon,
Inc in
December 1989
to provide
wastewater
treatment
services
and
have continued to
provide such services
for the
last
14
years.
During this
entire
time
period, I have served as lead process engineer on
all Noveon-Henry
Plant
matters in which
my firm
Brown
and Caidwell
has been involved. My firm was previously
known
as
Eckenfelder
Inc and
was acquired by Brown
and
Caidwell in
1998.
I received
two
degrees from Vanderbilt University. I received my Bachelor ofEngineering Degree in
Civil and
Environmental
Engineering in 1982 and my Master ofScience Degree in Environmental
and
Water Resources Engineering in
1984.
I
immediately
went to work forAWARE Incorporated in 1984
and
have remained
with
the same
•company for the last20 years in progressivelymore responsible positions
(from
project engineer to
project
manager
to
principal
engineer) in
the
area ofwastewater engineering (see Exhibit A for
resume documenting
this
experience). My firm has
changed
names twice. In 1989, we renamed
ourselves Eckenfelder
Incorporated in 1989 to honor Wes Eckenfelder
our Chairman
Emeritus
who is
still with
us today. Much ofwhat Ihave learned has been under Dr.
Eckenfelderas a
graduate student
and
as a co-worker. In 1998, Eckenfelder Inc was acquired by Brown
and CaidwelL
Duringmy career, I have personally conducted treatment
(treatability) testing of
industrial
wastewaters
and
contaminatedgroundwaters
and
developed treatment process design criteria from
test data. I have provided troubleshooting oroptimization services for wastewatertreatment
facilities
(WWTFs)
and
conducted waste
minimization studies.
I have also overseen the work
I

described
above, designed wastewater and contamina~ed
groundwater treatment processes, assisted
in effluent permit negotiations, supported expert testimony preparation and trained treatment plant
operators. I currently serve as lead process engineeron more technically challenging projects and to
train other engineers within the firm.
I am a licensed professional engineerin the states of Illinois, Michigan, Kentucky, and Tennessee. I
also am certified as aDiplomat in the American Academy of Environmental Engineers in the
specialty area of water supply and wastewater. This certification is held by less than 1300 people in
the United States and requires stringent peerreview and testing to acquire.
I have published 16
technical papers of which 7 are directly related to the Noveon-Henry Plant’s
issues andhave provided material for I textbook (Activated Sludge Treatment of Industrial
Wastewaters,John L. Musterman andW. Wesley Eckenfelder,Technomic Publishing Company,
1995). I also provided the technical reviewof a chapter from another textbook (“Granular Carbon
Adsorption ofToxics” from Toxicity Reduction in Industrial Efflu~nta~
PerryW. Lankford andW.
Wesley Eckenfelder, Van Nostrand Reinhold,
1992).
I have served as in instructor in numerous workshops including the following:
“Clarifier Operation and Maintenance” sponsored by Mississippi WaterPollution Control
Operators’ Associationin 1997;
“Aerobic Biological Treatment” sponsored by Tennessee State University in 1997,
1998, and
1999;
“Activated Sludge Treatment” sponsored by Brown and Caidwell and attended
by more than
10 industries during each offering in November 1999,March 2000, May 2001, November
2002, and November 2003; and
‘Wastewater Strategies for Industrial Compliance: Gulf Coast Issues and Solutions”
sponsored by Tulane University and Louisiana Chemical Association in December 2003.
Specific Design Experience Related to this Petition
I have developed the process design for following biological nitrification facilities. Eachof these are
fullyoperational today and meeting permit compliance.
P:\PROJ\23417
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2

Noveon-HenxyPlant Experience:
1989 to 2004:Have provided
the
followingassistance in chronological order listed below. I have
also spent acumulative of atleast 2 months onsite atthis facility throughout the years with no more
thantwo years
elapsing between visits. My last visit to the plant was in the Fall of 2003.
Optimization of WWTF operations.
Setup, conduct and oversight of treatability testing that was used to develop process design
of C-18 wastewater pretreatmentsystem andaeration basin upgrade. Testing was also used
to set allowable loading rates of various wastestreams,.
TrainWW~F
operators in process optimization and analytical testing.
Setup,conduct and oversight of treatabilitytesting that was used to develop conceptuallevel
design criteria for alternative processes for effluent ammonia-nitrogen reduction. Developed
conceptual level designs for these alternative processes. Worked with construction cost
estimators andvenders to develop conceptual level costestimates of these alternative
processes.
Provided as requested guidance to Noveon regarding WWTF operations and full-scale
testing ofprocesses and procedures intended to provide reduce effluent ammonia-nitrogen.
Authored or reviewed
all reports submitted to Noveon by Brown and Caidwell (formerly
AWARE Incorporated and Eckenfelder mc)
during entire period of 1987 through
2004.
Represented Noveon in discussions with IEPA regarding the Petition for an Adjusted
Standard.
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4

Noveon-Henry Plant Wastewater Treatment Facilities
Manyof the terms thatI haveused above and throughout this report are definedbelow as the
Noveon-Henry Plant WastewaterTreatment Facility ç~WTP)
is described. An understanding ofthe
WWTF is critical to understanding the evaluations conducted and the conclusions reached.
The wastewater treatment facility at the Henry Plant site is owned and operated by Noveon, Inc.
This facility treats wastewaters discharged from two manufacturing areas (resins and specialty
chemicals) that were once owned by BF Goodrich. BE Goodrich sold the resin business to the
Geon Companywho later sold
it
to the PolyOne Corporation. BE Goodrich sold the specialty
chemicals business and the
site’s wastewater treatment facility to Noveon, Inc. The wastewaters
discharged by Noveon comprise about 35 percent of the total dryweather flowrate to the WW’IF
with the remaining 60 percent being discharged from the PolyOne production areas.
Wastewaters from the Noveon-Henry Plant production areas discharge to one of two places as
illustrated in Figure
1. All wastewaters exduding those from C-I 8 manufacturing discharge
directly
to an equalization tank (the PC Tank), as shown in Figure
1. The wastewaters from C-18
FIGURE 1
BLOCK
FLOWDIAGRAM
OP
WASTESTREAM
SOURCES AND
wwrr
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ofNovo~ndoc
5

manufacturing discharge to apretreatmentsystem and are thenpumped to an equalization tank
(C-18 Tank). Prior work that I either conducted or oversaw definedthat the C-18 wastewaters were
causing the WWTF to be unable to comply with effluent BOD limits. These wastewaters contained
compounds that caused the bacteria responsible for organics removal, also known as BOD removal,
to slow down or become inhibited. This work also defined the pretreatmentof the C-18 wastewater
that would be required for the WWTF to treat these wastewaters while complying with effluent
BOD limits. Prior to installingpretreatment, the bulk ofthe C-18 wastewaterswere collected and
transported for off-site treatment and disposal. After this pretreatment was installed, the
pretreatment allowed the Noveon-HenryPlant to treat all C-18 wastewaters onsite while maintaining
compliancewith effluent BOD
limits. This pretreatment was not required of the other Noveon
wastewaters. This pretreatment also had no effect on effluent ammonia-nitrogen concentrations nor
would
it
have any such effect if applied to anyother Noveonwastewater.
Wastewaters from the PolyOne Plant production areas
discharge to one of two places as illustrated
in Figure 1. All wastewaters excluding those from 213 manufacturing discharge
directly to an
equalization tank (the PVC Tank). The wastewaters from 213 manufacturing discharge to a
pretreatment systemand are thenpumped to same equalization tank (PVC Tank). Prior work by
others had indicated that the 213 wastewaters were causing the WWTF to be unable to comply with
effluent Biochemical Oxygen Demand (BOD) and Total Suspended Solids (~SS)
limits. These
wastewaters contained compounds that kept solids from settling in the primary and secondary
clarifiers as well as fine solids that passed through the WWIF. Pretreatment was installed to mitigate
these affects. It has been successful in allowing the Noveon-Henry Plant to treat all 213 wastewaters
onsite while maintaining compliancewith effluent BOD and TSSlimits. This pretreatment was not
required of the other Polyone wastewaters. This pretreatment also had no
effect on effluent
ammonia-nitrogen concentrations norwould
it
have any such effect if applied to anyother Polyone
wastewater.
Stormwater from the both the Noveon and PolyOne sites and discharges from cooling towers,
boilers, and riverwater treatment are discharged to the Storm/UtilityPond (the “Pond”)
as
illustrated in Figure
1. A portion of the Pond contents are pumped through a filter to removeTSS
prior to discharge the Illinois River. The remaining portion is pumped to the PVC Tank for
subsequent treatment. The amount of Pond Water returned to the PVC Tank is a function of the
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6

capacity of the filter treating the Pond Water, the PVC Tank operating level, and the need for other
wastewaterto compliment the required PC Tank discharge flowrate. The PVC Tank has a minimum
allowable operating level, below which the tank mixer shuts off. Work thatI have conducted and
overseen hasindicated that the PC Tank discharge must be limited to approximately 23 percent of
the combined influent flow to the aeration basins to maintain compliancewith effluent BOD limits.
The PC Tank discharge contains compounds that can inhibit or slow down the bacteria responsible
forBOD removal if their concentrations
are allowed to exceed certaincritical concentrations. So the
amount of Pondwater diverted to the PVC Tank forsubsequent treatment increases duringawet
weatherperiod when the capacity of the filter on the pond discharge is approached, when the PVC
Tank level nears its minimumoperating level, andwhen the flow contribution of the PC Tank
discharge approaches 23 percent. The contents of the PVC Tank, PC Tank, and C-18 Tank are
pumped to a pH adjustment tankalong with groundwater from arecovery well (Well No.
3). The
pH of the combined wastewater is adjusted. Coagulant and polymer are added to the combined
wastewater to assist in removing solids from the combined wastewaterin the sedimentation basin
(also known as primaryclarifier). The solids settle for approximatelyone hour in the primary
clarifier. The settled solids then combinewith solids discharged from the bottom of the second
sedimentationbasin (also known as the secondary clarifier) and are dewatered usinga filter press.
The dewatered solids are disposed in a permitted off-site landfill. The
filtrate from sludge dewatering
is returned to the PVC Tank for reprocessing through the WWTF. When the filter press is not
operating, the sludge from the primary clarifier underflow is pumped back to the PVC Tank for
reprocessing in the WWTF and sludge discharge
from the secondary clarifieris ceased.
The effluent from the primary clarifieris pumped to four aeration basins (2.0 million gallons
combined volume) that operate in parallel. These basins are aerated to mix the tank contents and to
maintain a minimum operating dissolved oxygen concentration of 1.5 mg/L. Sludge is returned
from the bottom of the secondary clarifier to keep these tanks supplied with an acclimated culture of
bacteria. pH is controlled as needed to maintain an optimumrange forbacterial growth (pH 6.5 to
pH 8.5). The bacteria grown in this tank remove organic compounds with the aid of dissolved
oxygen, ammonia-nitrogen, and phosphorus. In the process of this removal these bacteria also break
away ammonia-nitrogen from organic compounds containing amines (also known as organic
nitrogen compounds). Both biological treatment steps
are illustrated
below. Dissolved
oxygen
needed for biodegradationis provided by the aeration equipment. The two predominantnutrients
P:\PROJ\23417
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Noveondoc
7

required for biological degradation axe ammonia-nitrogen and phosphorus.
Ammonia-nitrogen is
presentin the wastewater and is formed through degradation of the organic nitrogen in the
compound. Phosphorus is added to the return sludge going back to the aeration tanks.
BiologicalTreatment Reactions
Organic compounds (measured as BOD, Biochemical OxygenDemand)
+
Ammonia-Nitrogen
+
Phosphorus+ Dissolved Oxygen
+
Bacteria yields MoreBacteria (reproduction and growth)
+
Carbon Dioxide
÷
Water
Organic Nitrogen (an organic compound with essentially ammonia-nitrogen attached)
+
Phosphorus+ Dissolved
Oxygen
+
Bacteria yields Organic Compound
+
Ammonia-
Nitrogen...The Organic compound then gets degraded justlike above using some of the
ammonia-nitrogen generated.
The bacteria stayin the aeration tanks about 2.5 days where theydegrade organic compounds and
organic nitrogen. They are thendischarged through aline where they get conditionedwith polymer
to help them
settle better in the secondary clarifier. They settle approximately3 hours in the
secondary clarifier. They are removed continuously offthe bottom of the darifler andsent back to
the aeration tanks to degrademore organic compounds and organicnitrogen. A portion of the
bacteriais removed from the system (termed “sludge wasting”) to control population growth and
keep the average
age of the bacteria (the Mean Cell Residence Time) and Food-To-Mass (F/M) ratio
in an optimal range. The bacteria removed from the system are discharged to the filter press for
sludge dewateringand subsequent off-site disposal in alandfill.
The treatment described includes pretreatment, primary treatment (pH adjustment,
coagulation and
primary clarifier), and secondary treatment (aeration and secondary clarifierwith sludge return). This
treatment is defined by USEPA as the “Best Available Technology Economically Available” for the
Organic Chemicals, Plastics, andSynthetic Fibers industrial category (Code of Federal Regulations
Title 40, Part 414.83, Subpart H).This industrial categoryincludes Noveon and PolyOne. However,
Noveon treats the
wastewater even furtherby discharging the effluent from the secondary clarifier
to a filter to remove additional solids. This additional treatment process is termed tertiary treatment.
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8

Noveon also filters the water coming out of the Pond to remove solids. These two filtered
wastewater streams combine and discharge through the effluent compliance point that Noveon
monitors for flow and regulated compounds such as
specific organics, BOD and TSS.
The design and operation ofNoveon’s WWTF are compatible with conditions defined by 35 ILL.
Admin. Code 370.920,35 ILL. Admin.
Code 370.1210,
and Ten State Standards
to grow
nitrifying
or ammonia-degradingbacteria as illustrated below in Table
1. However, they do not grow. The
Illinois regulations cited and the Ten State
Standards are design and operating standards that are
intended to promotecomplete nitrification in municipal wastewater treatment facilities. These
standards are intentionally excessive (or conservative) and allow for a significant margin of error in
waste load determinations and operating conditions based on my experience. There are no
Illinois or
Ten State standards
for single stage nitrification of industrial wastewater treatment facilities since the
nature of these wastewaters varies from industry to industry. These industrial designstandards are
developed on a site specific basis usingwastewater characterization data,
treatability testing, and
professional experience.
Nitrifying or ammonia-degrading bacteria are much more sensitive than theb~cteria
that degrade
organic compounds and organic nitrogen. There are compounds presentin the Noveonwastewater
that prevent or inhibit their growth. If the bacteriawere not inhibited and could grow in the aeration
tanks theywould provide ammonia removal in the same tankage as the other bacteriause to provide
organics removal. Consequently, the treatment would be termed single stage nitrification since in the
same tankage (same
stage) both organics removal andammonia removal occur. If you were to grow
these ammonia-degradingbacteria in a system downstream-ofthe secondary clarifier, it would be
called tertiary nitrification. These nitrifying bacteriagrow in the manner described
as
follows:
BiologicalTreatment Reaction
Ammonia-Nitrogen
+
Phosphorus+ Dissolved
Oxygen
+
Alkalinity
+
Bacteria yields More
Bacteria (reproduction and growth)
+
Nitrate-Nitrogen
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Table 1. Comparison ofIllinois Standards,
10
State
Standards, and
Noveon-Henry Plant
Conditions for Single Stage Nitrification
Condition
Illinois
Standarda
Ten State
Standard”
-
Noveon
PlantC
Aeration Tank Loading, lbs BOD/day per
1000 cu ft
~15
~15
14
Aeration Basin Mixed
Liquor DO, mg/L
?~2
?~2
?~2
Aeration Basin Mixed Liquor
pH,
s.u.
7.2 to 8.4
Not Defined
6.8 to 7.2
Sludge Age,
days
?..20
Not Defined
?~40
Aeration Basin Mixed LiquorTemperature, degrees F
?
50
Not Defined
?
80
Aeration Basin Average Hydraulic Residence Time, days
?
0.33
Not Defined
2.5
Aeration Basin F/M Ratio, lbs BOD/day per lb MLVSS
Not Defined
0.05 to 0.10
0.10
ReturnActivated Sludge Flow,
of Ave Influent Flow
15 to 100
50 to 200
100
‘IllinoisAdministrative
Code, Title 35, Subtitle C, Part370, Subpart I, Title 370.920 and Subpart L,
Title 370.1210. Both govern municipal (notindustrial) W\VTF design.
~ Recommended Standards forWastewaterTreatment Facilities, 1997 Edition, Wastewater
Committee of The Great Lakes-Upper Mississippi River Board of State and Provincial Public
Health and Environmental Managers (includes Illinois), Chapter90. These standards are
to
provide guidance in the design of municipal (notindustrial) WWTF design.
C
1999 through 2004.
Applicability of35
ILL.
Admin. Code 304.122: The
provisions of Illinois Title 35, Subtitle C, Part
304, Subpart A, Section
304.122 (35 ILL. Admin. Code 304.122) is stated as
follows:
a)
No effluent from any source which discharges to the Illinois River, The Des Plaines River
downstream of its confluence with the Chicago River System or the Calumet River System,
and whose untreated waste loadis 50,000 or more population
equivalents shall contain more
than 2.5 mg/L of total ammonia nitrogen as N during the months ofApril through October,
or 4 mg/L atother times.
b)
Sources discharging to any of the above waters and whose untreated waste load cannot be
computed on apopulation equivalent basis comparable to that used for municipal waste
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10

treatment plants andwhose total ammonia nitrogen as N discharge exceeds 45.4 kg/day(100
pounds per day) shall not discharge an effluent of more than 3.0 mg/L of total ammonia
nitrogen as N.
c)
In addition to the effluent standards set forth in subsections (a) and (b) of this Section,
all
sources are subject to Section 304.105.”
Section 304.105 states “In addition to the other requirements of this Part, no effluent shall, alone or
in combination withother sources, cause aviolation of any applicable water qualitystandard.”
Noveon has retained another expert (e.g., Mike Corn, P.E. of AquAeTer) that will testify that
Noveon can andwill comply with water quality standards (section 304.122c) in the Illinois River for
ammonia-nitrogen if theyare allowedto install an effluent diffuser. Noveon has requested IEPA to
grant approval of such installation and is committed to such installation once approval is granted.
An effluent diffuser will more uniformly distribute the discharge of the Noveonin the Illinois
River.
The remainder ofmy testimony is based on Noveon’s compliancewith Section 304.122c.
In my professional opinion, Sections 304.122a and 304.122b do not apply to the Noveon-Henry
Plant discharge
forseveral reasons.
The Noveon-Henty Plant untreated waste loadcan be “computed on apopulation
equivalent basis comparable to that used for municipal wastewater treatment plants”.
Consequently, 304.122b does not
apply. In my opinion, the word “comparable” merely
questions whether the data existto express an untreatedwaste load in population equivalents
like one does when either designingor evaluatinga municipal wastewater treatment plant.
The data do
exists and such calculations can be and have been made. The results from such
calculations allow one to put the Noveon-HenryPlant’s untreated waste load in a
perspective others can readily understand (population equivalents). The term “population
equivalent basis” is intendedto put the relative size of an untreated waste load in
perspective. The term was never intended to describe howthe waste load was to be treated
but only the magnitude of the waste load
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There are sources that could discharge to ariver for which “apopulation equivalent basis
comparable to that used for municipal waste treatment plants” could not be computed.
These would be discharges for which data could not be gathered to calculate population
equivalents. TEPA usesBOD, TSS, and flow fordetermining population equivalents.
Presumably these discharges would be those forwhich BOD,TSS, and flow could not be
reliably determined. This is not the casewith the Noveon-Henry Plant discharge.
An untreated waste loadcan be and has been calculated by myselfand JEPA for the
Noveon-Henry Plant discharge on “a population equivalent basis comparable to that used
for
municipal waste treatment plants”. The correct results from these calculations are stated
below and dearly define the Noveon-Henry Plant discharge
as havingless than 50,000
population equivalents. Consequently, 304.122a does not apply.
Since Sections 304.122a
and 304.122b do not apply, the Noveon-I-Ienry Plant is not
required to provide additional effluent ammonia-nitrogen removal. Furthermore, the
As stated above, correct calculations clearly define the Noveon-HenxyPlant discharge
as having less
than 50,000 population equivalents. IEPA has calculated the population equivalents of the
Noveon-Henry Plant for flow and BOD (Response to First Set ofInterrogatories of Noveon, Inc.
to Illinois Environmental Protection Agency,pages 4 and 5) based on data provided in the Baxter
and Woodman-Wastewater Treatment Plant Report datedJune
1994. This report did not present
anydata on the combined untreatedwasteload. The report discussed the wasteload fed from the
equalization tanks to the primary clarifier. However, this wasteload contains wastestreams that are
internal to the WWTF that add flow, BOD, and TSS including primary clarifier sludge
when sludge
dewateringis not occurring, filtrate from sludge dewatering, and backwash water from the tertiary
(secondary clarifier effluent) filter. Even with this addition, IEPA calculated flow and BOD
population equivalents of 916 and 19,412, respectively (page 4). I corrected the population
equivalent calculation for TSS based on data collected by Noveon duringthe period ofJuly 2002
through June 2003. The corrected value was 24,955
as illustrated belowand in Figure
1. This
calculation depends upon
calculating the untreated waste load TSS coming to (not recyclingwithin)
the W~TFfrom all
sources:
PC Tank, PVC Lift Station Discharge which represents the waste load
discharged from the PolyOne production areas, the 213 wastestream waste load before
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pretreatment, the PC Tank discharge, and the C-18 Tank discharge (pretreatment does not change
the flow or TSS of this discharge but does increase its BOD). The TSS dischargedby the combined
Well No.
3
and Storm/UtilityPond discharges are less than 25 percent of the total influent
wasteloadas
illustrated in the Baxter and Woodman report.
PVC
Lift Station Discharge Averages(not the PVC Tank Discharge Averages presented in Baxter
andWoodman Report): 133 gptn,
1957 mg/TSS,and 3123
lbs/dayTSS
PC
Tank Discharge Averages: 94 gpm,
900
mgfL TSS, and 1015 lbs/day TSS
C-18
Tank Discharge Averages: 3.6 gpm,
300
mgfL
TSS,
and
13
lbs/day TSS
213 Averages (includedin PVC Tank Discharge data presented in Baxter and Woodman Report):
35 gpm,
2000 mg/L TSS (estimate), and 840 lbs/day
TSS
(estimate)
Total:
4991
lbs/dayTSS or apopulation equivalent (PE) of4991
lbs/day TSS divided by
0.20
lbs/day TSS per person(capita) or 24,955
population equivalents. This is much less than PE
of
265,000 calculated
by
IEPA in the Response to First Set of Interrogatories
ofNoveon, Inc.
to Illinois Environmental Protection Agency, pages 4 and
5. The reason for this large
discrepancy is due to recycle solidsincluded in the JEPA calculation. These solids stay within
the WWTF and are not part of the untreatedwaste load for which these calculations are
reserved.
Even though not apart of the IEPA’s definition of “population equivalent”, population equivalents
can also be calculated based on ammonia-nitrogen and Total Kjeldahl Nitrogen (~KN)loads that
are really the thrust of 35 ILL. Admin. Code 304.122. TKN is the summation of ammonia-nitrogen
and organic-nitrogen. The wasteload used to develop all
effluent ammonia-nitrogen reduction
options included average loadings of 385 lbs/day ammonia-nitrogen and 1038 lbs/day Total
Kjeldahl Nitrogen (TKN). Based on population equivalent factors of 0.019 lbs ammonia-nitrogen!
capita per day and0.029 lbs TKN/capita per day (see Wastewater Engineering: Treatment and
Reuse: Metcalf and Eddy, Inc., Fourth Edition, page 182), the Noveon-HenryPlant population
equivalents would be 20,263 and
35,793,
respectively.
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In my professional opinion, all correct and relevant population equivalentcalculations forthe
Noveon-Henry Plant place it under 50,000 population equivalents rendering 35 ILL. Admin. Code
304.122a and 304.122b not applicable.
Highlights ofEffluent Ammonia-Nitrogen Reduction Evaluations atNoveon-Henry Plant
It is my professionalopinion that 35 ilL
Admin. Code 304.122a and 304.122b do not apply.
Consequently, no effluent limitations and therefore no additional effluent ammonia-nitrogen
reductions are required.
The Noveon-Henry Plant currently provides effluent ammonia-nitrogen reduction through source
control and removal
associated with
BOD
removal nutrient requirements. However, in an effort to
resolve disputes with the IEPA, Noveon retained Brown and Caldwefl (where I serve as lead
engineer) to evaluate whether there were any feasible technologies that would provide additional
effluent ammonia-nitrogen reduction.
Both Noveon and Brown and Caidwell have extensively
evaluated additional effluent ammonia-nitrogen reduction over the last 14
years.
All statements made belowrepresent my understanding of the issues and my professional opinion
regarding these issues.
1.0
Unique Characteristics ofthe Noveon-Henry Plant
and
its Associated Wastewaters:
In my professional opinion, several factors make the Noveon-Henry Plant andits associated
wastewaters unique as
it
relates to the Petition for Adjusted Standard. These factors make the
wastewaters at The Noveon-Henry Plant more difficult and more costly to treat than either
municipal wastewaters or most other industrial wastewaters. These factors are listed below.
First, IEPA has reported that there are only three other plants in the country that generate a similar
wastewater. Two of these three plants discharge to a Publicly Owned Treatment Works. Only one of
these plants discharges directly to areceiving water. So, the wastewater is not commonly found.
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Second,
the building block of Noveon’s main product line at the
facility (rubber accelerators) is
MBT (mercaptobenzothiazole). As a building block,
it
is present in numerous wastestreams
throughout the plant sewer system. It is also a well-recognized inhibitor of biological nitriflcation
even at trace levels of 3 ppm as reported by M.L. Hockenbury and C.P.L. Grady in the Journal of
the WaterPollution Control Federation in 1977 (see Exhibit B). This compound is poorly
degradable as you would hope for a rubber-making additive. No consumerwants to buy readily
degradable tires and other rubber products. Because ofits poor degradability, MET is used as an
additive to nitrogen fertilizers to inhibit biological nitrification in the soil so that more ammonia
nitrogen will be available to the crops (seeExhibit B for article publishedin the National Corn
Handbook, February 1992). However, the large use of this inhibiting compound in production atthe
Noveon-Henry Plant make the most widely practiced and least expensive ammonia-nitrogen
removal process
(single stage nitrification)
unavailable atthe Noveon-HenryPlant. MET removal is
provided in the WWTF Noveon-Henry Plant, just not to the trace levels required to initiate
biological nitrification. Consequently, atypicaland expensive processes would be required to reduce
effluent ammonia-nitrogen concentrations.
Third, the Noveon-Henry Plant and PolyOne Plant contain wastestreams that require pretreatment
aheadof the onsite biological treatment plant to preventprocess upsets and non-compliance with
effluent BOD andTSS limits. Consequently, there is an inherent unreliability with any biological
treatment process used onsite whether it
is
used for BOD removal or nitrification.
Fourth, the Noveon wastewater contains several degradable organic nitrogen compounds such
as
tertiary butyl amine. When these compounds are degraded, theyrelease ammonia-nitrogen.
Consequently,
the effluent ammonia-nitrogen concentration increase as the presence of these
compounds increase in the influent wastewater and as these compounds are more thoroughly
biodegraded. This explains why the influent ammonia-nitrogen concentration at the Noveon-Henry
Plant is much less than the effluent concentration (less than40 mg/L versus greater than 80 mg/L).
Consequently, the majority of the effluent ammonia-nitrogen atThe Noveon-Henry Plant is due to
thorough biological treatment oforganic compounds.
Fifth, the compounds presentin the Noveon-HenryPlant wastewater make oxygen transfer into this
wastewater about half as efficient as municipal wastewater as measured
by a parameter known as
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“alpha”. Alpha is the ratio of oxygen transfer in wastewater divided by the oxygen transfer in
tapwater. In municipal wastewater this alphavalue for fine bubble diffused aeration is typically
0.60 versus
the 0.35 measured in the Noveon-Henry Plant wastewater in 1987 by Gerry Shell
Consequently, the Noveon-Henry Plant has to use about twice the horsepower to transfer the same
amount of oxygen atmunicipal wastewater treatment plants. Furthermore, thisincreased power has
to be accompanied by increased aeration tankage to keep operatingpower levelsin a reasonable
range.
Sixth,the Noveon-I-lenry Plant wastewater is lightly buffered. Consequently, if biological
nitriflcation could be implemented with inhibitor control,the majority of alkalinity would have to be
added whereas in biological nitrificationof municipal wastewater the majority (lf not all) of the
alkalinity required is present in the wastewater.
Eighth, the Noveon-Henxy Plant does not have any additional appreciable power available atthe
WWTF. Any significant additional power required at the WWTF would require installation of a new
motor control center and installation of anew power line to a substation located approximately
0.5 milesaway. Consequently, any WWTF upgrade (regardless of magnitude) to address effluent
ammonia-nitrogen reduction will require a significant cost ofpower delivery.
2.0
History ofEffluent Ammonia-Nitrogen Reduction Evaluations at the Noveon-Henry
Plant
During the last
14 years, Noveon andBrown andCaidwell haveconducted extensively evaluated
whether therewere any feasible technologies that wouldprovide additional effluent ammonia-
nitrogen reduction at the Noveon-HenryPlant. These evaluations have consisted ofliterature
review, consultationwith additional experts, laboratory-scale treatment investigations, full-scale
operations and capital enhancements, and full-scale plant trial investigations. Many of these
evaluations were based on results of prior evaluations in an attempt to continue to build on findings
ofprior evaluations. In
my professional opinion, there havebeen “norelevant stones left unturned”.
The significant evaluations in which
1 have participated are summarized below.
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2.1
Single Stage Nitrification, Powdered Activated Carbon Addition, EffluentIon
Exchange
and
Tertiary
(Effluent) Nitrification
When I first got involved atthe Noveon-Henry Plant in 1989, the focuswas on developinga
strategy for achieving
consistent effluent BOD compliance. Brown and
Caldwefl conducted
continuous flow treatability testing, that I designed and oversaw, that indicated this compliance
could be achieved with pretreatment of one major wastestream
(C-I 8). During
the course of the
treatabillty studies,
we noticed that the WWTF would discharge elevated
concentrations of
an-unonia-nitrogen while providing
excellentBOD removal. Despite carefully controlled conditions
of F/M, MCRT, pH, temperature
and
DO that should prompt
biological nitrification, none was
observed. This indicated that MET and possibly other bio-inhibitors were present in the influent at
sufficient levels to prevent biological nitriflcation. Batch testing was conducted in early 1989 to
determine ifpowdered activated carbon (PACt)
could be added to remove these
inhibitors and allow
biological nitrification. Furthermore, batch testing also evaluated
selective ion exchange treatment
(dlinoptilolite)
of the effluent,
and tertiary (effluent) nitrification of the effluent. This work indicated
that an untenable, large dose of PAC would be required to allow single stage nitrification
(5000mg/L or 17 tons/day). Because of this finding (untenable carbon usage) and
the
certainty of
fouling problems, no furtherconsideration was given to carbon treatment
.
This
work also indicated
that even the most appropriate ion exchange was not
selective for ammonia-nitrogen removal due to
the other competing cations in the wastewater (approximately 100 pounds resin required to remove
1 pound ofammonia-nitrogen). Lastly, thiswork suggested that the effluent could be biologically
nitrifled with yet another or tertiary treatment unit. Consequently,
subsequent evaluations
considered more thoroughly tertiary nitrification.
2.2
Further Evaluation of
Tertiary
Nitrification
andPretreatment with Single Stage
Nitrification
Based on these results, Noveon’s corporate Research and Development group initiated a continuous
flow treatability study that focused on tertiary nitrificationwith alkalinity addition. This work was
conducted over about a 6 month period using fixed film biological nitrification and secondary
clarifier effluent samples that were collected monthly. The work indicated that tertiary nitrification
could be accomplishedand low discharge ammonia-nitrogen concentrations
(less than 6 mg/L)
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could be achieved with alkalinity addition and effective performance of upstream treatment
processes. Therewere legitimate concerns about how reliably this process would have performed
under the daily variability of secondaryclarifier effluent quality.
Brown and Caldwell also initiated a series of batch treatabilitytests that I designed and oversaw.
This testing was to identify if available technologies could be used to remove the bio-inhibitors
presentin the influent wastewater to the extent that the most widely practiced and least expensive
ammonia-nitrogen removal process (singie stage nitrification) could be employed. These treatabillty
tests evaluated hydrogen peroxide treatment, clay absorption,
and precipitation. However, the rate of
biological nitriflcation was
slower than would be expected for an uninhibited
system indicating that
bio-inhibitors were still presentin the effluent from the treatment plant This work indicated that
precipitation and filtration of the Noveonwastewater atpH 2 would allow single stage nitrification
to proceed. However, this pretreatmentwould require significant acid addition to lower the
wastewater pH from pH
10 to pH 2 and then significant alkali addition to increase the pH from
Ph 2 to pH 7 forbiological treatment The precipitant from the pH 2 pretreatment was
analyzed and
found to be predominantly
MET
(a known nitrificationinhibitor).
2.3
Further Evaluation
of Pretreatment (p112 Precipitation
and
Solvent Extraction) and
Single Stage Nitrification
Based on results of the work described above, Brown and Caldwell conducted a continuous flow
treatability study, which I designed and oversaw, to evaluate pH 2 pretreatment of the PC
wastewater and singie stage nitrification. This studyindicated that singie stage nitrification could be
achieved with this pretreatment. The rate of nitrificationwas inhibited indicating that some
bio-inhibitors still remained in the combined influent. Effluent
ammonia-nitrogen concentrations
from this process varied from I mg/L to 20 mg/L, indicating a variation in remaininginfluent
bio-inhibitor concentrations. It was concluded that this pretreatment process would support single
stage nitrification. However, effluent ammonia-nitrogen concentrations
would not consistently
achieve those limited by 35 ILL. Admin. Code 304.I22a or 304.122b.
During this same period
of time, Noveon investigated a process used in Germany for MET
recovery. This process used solvent extraction. Results of this investigation reportedly indicated that
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the process would pose safety concerns (potential forexplosions) and would also be costprohibitive
to implement at the Henry Plant (reportedlygreater than $10 million).
2.4
Assessmentof WWTF for Compliance with Conventional Design for Single Stage
Nitrification 35
ILL. Admin.
Code
370.1210 and
370.920
Noveon retained Baxter andWoodmanin
1994 to review the WWTF for compliance with
the
Illinois design standards for single stage nitriflcation of municipal wastewaters. These standards axe
intentionally excessive (or conservative) and allow for a significant margin
of
error in waste load
determinations andoperating conditions based on my experience. There are no Illinois design
standards for single stage nitriflcation of industrial wastewaters.
These industrial design standards
are developed on asite specific basis usingwastewater characterization data, treatability testing,
and
professional experience.
The reviewby Baxter and Woodmanindicated the WWTF would comply with
the
municipal
wastewater standardswith the addition of about
65 percent more aeration tankage. I was convinced
that the WWTF would not provide single
stage nitrificationwith this additional aeration tankage.
However, Noveon expanded the aeration tankage in 1998 by
100 percent to provide greater aeration
capacity and greater treatment plant flexibility. This addition put the WWTF in full compliance with
35 ILL. Admin. Code 370.1210 and 370.920 and Ten State
Standards (which includes Illinois) for
single stage nitriflcationand yet the WWTF did not exhibit anynitrification. The reason nitrification
was not achieved was not due to a lack of equipment, but rather the presence of bio-inhibition.
2.5
Alternative Bacteria
IEPA had conducted aliterature search and found an artide that seemed to imply that special
bacteria could be grown in the Noveon-Flenry Plant that would both degrade the difficult
compounds (such as morpholine) and remove ammonia-nitrogen atthe same time.
I explained to
IEPA that these were not the findings of this article. However, IEPA was persistent that these
bacteria could achieve both types of degradation (morpholine and ammonia-nitrogen).
Consequently, Noveon brought in the author of this article from England (Dr. Jeremy Knapp).
Dr. Knapp reviewed the Noveon-Henry Plant operation. He then explained that the bacteria that he
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wrote about were already presentin the Noveon-HenryPlant based on morpholine removal data he
had reviewed and that the conditions present in the Noveon-Henry Plant were suitable for
maintaining aculture of these bacteria. He further explained that these bacteria do not provide
nitnification. He also explained that the Noveon-HenryPlant provided
all the right conditions for
single stage nitrificationifbio-inhibiting compounds were not present
Noveon on
several occasions has tried adding specialty bacteria to removedifficult to degrade
compounds. During these same periods, Noveon has added nitrifying bacteria from the Peoria
P01W. In no instance has Noveonbeen able to initiate nitrification. This indicates that the lack of
nitrificationis due to inhibitors that are not degraded within the confines of the Noveon-Henry
Plant evenwith special bacteria addition. Furthermore, this Plant offers the biological treatment
opportunity that is required by Ten State Standards and 35
ILL. Admin. Code 370.1210 and 370.920
for single stage nitrification.
2.6
Numerous Occasions
of
Seeding Plant with Nitrii~ting
Bacteria
The Noveon-Henry Plant has been in compliance since 1998 with Ten State
Standards and 35
ILL.
Admin. Code 370.1210 and 370.920for single
stage nitrification. Since this time, Noveon has added
on numerous occasions bacteria from other WWTF that are activelynitrifying. These additions were
intended to improve the Noveon-HenryPlant WWTF performance. Yet, in no case has nitrification
occurred at the Noveon-Henry Plant despite optimum conditions of MCRT (greater than 30 days),
temperature (28 to 32 degrees C), pH (6.8 to
7.5), DO (greater than 2 mg/L).
Again,
it
is my
professional opinion that this is due to the presence of bio-inhibitingcompounds in the influent.
2.7
Full-Scale Plant Trial
of
Alkaline Air Stripping to Achieve Effluent Anirnonia-
Nitrogen Reduction
The Noveon-Henry Plant conducted a full-scale trial of alkaline air stripping of the combined
influent. This required Noveon to
set up an interim pumping system, caustic addition system, and
acid addition system. This interim system diverted all primary clarifier effluent (approximately
560 gallons per minute) to an aeration basin that had been set
aside for this testing.
Caustic was
added to the aeration basin to maintain a target pH value of 10.5. A surface aerator was placed in
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this basin and operated to assistin air stripping. Effluent from this tank was diverted to a blend tank
where the pH was
lowered. The blend tank contents were thenpumped to the ~ther three aeration
basins forbiological treatment. This treatment did demonstrate a modest reduction in effluent
ammonia-nitrogen (less than 20 percent). This reductionwas low, in my opinion, due primarily to
the fact that the majority of the effluent ammonia-nitrogen is formed during biological treatment.
Secondly, the pH control method was unable to consistently keep the tankcontents at or above
pH 10.5.
2.8
Full-Scale Trial of Pretreatment and Single StageNitrification
Noveon environmental staffconducted a literature search and found an article that indicated that
MET could be co-precipitatedwith ferric hydroxide at an elevated pH (seeExhibit B). The
article
indicated that significant removal could be accomplished at pH 4.5 versus the pH 2 pretreatment
evaluated by Brown and Caldwell. Noveon conducted a full-scale trial
of
this pretreatment system in
hopes of achievingsingle stage nitrification.
I reviewed the article, believed their was a likelihood
of
success in this trial, helped design the trial conduct, reviewed data from the trial and witnessed this
trialin progress. The trial involved Noveon installingan interim precipitation system and separate
sludge dewatering system to treat and segregate pretreatment byproducts (sludge and filtrate from
sludge dewatering). The entire PC wastewater discharge (120 gpm) was routed
through this system
involving ferric chloride addition to lower the PC Tank wastewater to pH 4.5. The pH adjusted
water was allowed to separate in interim claniflers. The treated wastewater was transferred usingan
interim pumping system to the existingprimary treatment system. The precipitated sludge was
dewatered using an interim filter press with precoat addition
system. The filtrate from sludge
dewatering was routed back to the pretreatment system. The pretreatment system was operatedfor
months and did demonstrate significant MBT removal
(greater than 50 percent). At the end of this
operatingperiod, Noveon brought in a tanker load (5000 gallons) of bacteria from a plant in Indiana
that had a high population ofactive nitrifyingbacteria. The bacteria were added to the aeration
basins. The pretreatment system continued to operate while Noveon checked
for signs of
nitrification in the activated sludge system. The activated sludge system was operated under adequate
DO, pH, MCRT and alkalinitycontrol to prompt nitrification. No nitrification occurred despite this
large investment of resources (greater than $100,000) and time (greater than 4 months). Itis my
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opinion that nitrification did not occur because of the continued presence of bio-inbibiting
compounds in the influent (MBT and likely others).
2.9
Consideration ofOther Lesser Known Technologies
Another consultant (Ecology and Environment,
mc)
was retained to review the work of Brown and
Caldwell for Noveon. This consultant believed that all feasible technologies had been considered for
effluent ammonia-nitrogen reduction excluding ozonation. A conceptual level design and cost
estimate was developed forthis treatment process.The processwould presumably achieve a
98 percent reduction in effluent ammonia-nitrogen but at a present worth cost of $20.32 million
(almost twice the cost of any other process considered). This processwould also significantly
increase the effluent total dissolved salt concentration due to the caustic addition required to
neutralize the acid generated from this process.Additionally, a significant substation upgrade would
be required to deliver the additional power consumed (equivalentto approximately 3500 hp
demand).
I discovered in 2003 a company in Memphis, Tennessee that had apatented membrane that
selectively
separatedammonia-nitrogen from wastewater containing little other constituents besides
ammonia-nitrogen. This membrane was tested to remove ammonia-nitrogen from alandfill leachate
and groundwater stream that was less concentrated in other constituents than the Noveon
wastewater. The company conduded after actual testing that the membrane would not be suitable
for treating the leachate
and groundwater stream due to interference caused by other compounds
presentin the wastestrearn. Consequently, I did not further pursue use of this membrane at the
Noveon-Henry Plantfor effluent ammonia-nitrogen reduction.
2.10
Comparative Performance and Costs of
all Proven Effluent Ammonia-Nitrogen
Reduction Processes
After approximately 14 years of extensive evaluations
by Noveonand Brownand Caidwell,
all
applicable treatment processes, in my professional opinion, have been considered for effluent
ammonia-nitrogen
removal. Treatment processes considered went beyond those included in the
USEPA Process Design Manual: Nitrogen Control (EPA 625R93010). No stone has gone unturned.
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The proven treatment processes described above have beendeveloped by me and support staffwell
enough to accomplish the following.
predict potential effluent ammonia-nitrogen reduction,
understand the pros andcons,
develop conceptual level designs for their application, and
develop conceptual level design cost estimates (capital, annual, and presentworth costs) for
these treatment aiternatives to within
30 percent accuracy usingavailableinfluent waste load
data.
The proven treatment processes that were evaluated are listed below.
Alkalineair stripping (air stripping atpH 10.5) of PC Tank contents with off-gas collection
and treatment. Noveon believed this off-gas collection andtreatment would be required to
comply with air quality regulations. At high pH ammonia-nitrogen exists as agas dissolved in
liquid and can be removed from the liquid by air stripping.
Alkaline air stripping of
PVC
Tank contents.
Alkaline air stripping
of
secondary clarifier effluent.
Struvite precipitation of combined influent prior to primary clarification. Ammonia-nitrogen
can be precipitated as NFI4MgPO4(H2O)6.
Breakpoint chlorination of secondary clarifier effluent. The addition ofchlorine converts
ammonia-nitrogen to nitrogen gas that exits the liquid to the atmospherewithout the need
forair stripping.
Nitrification of PVC Tank wastewater (non-PC wastewaters).
Nitrificatiori is a process by
which bacteria convert ammonia-nitrogen to nitrate-nitrogen. The bacteria consume large
amounts ofoxygen
(4.6 lbs oxygen/lb ammonia-nitrogen
removed) and alkalinity (7.14lbs
alkalinity/lb ammonia-nitrogen removed).
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Nitrification of the combined wastewater. This process would require pretreatment of the
PC wastewater to remove
bio-inhibitors.
Nitrification of secondary darifler effluent
(tertiary thtrification).
Ion exchange treatment of the final effluent. Ion exchange is a process where another cation
(e.g., sodium (Na4) or hydrogen (H4) is released from a resin into the water so another
cation (NH44)
can be removed from the water.
The treatment process evaluation described above is briefly summarized in Exhibits C, D, and E.
This evaluation established that the processoffering the lowestpresentworth costfor reducing
effluent ammonia-nitrogen was
alkaline stripping of the PC Tank contents ($2.31
million). This
alternative howeverwould only provide a 27 percent reduction in effluent ammonia-nitrogen. If
35 ILL. Admin.
Code 304.122b was applicable, and I strongly believe that itis not, the average
effluent ammonia-nitrogen would have to be reducedby 98 percent (135 mg/L reduced to 3 mg/L).
Under peak effluent conditions, the effluent ammonianitrogen reduction would have to exceed
98 percent. The process offering the lowest present worth
cost thatwould be capable of
meeting the
98 percent reduction requirement was ion exchange ($5.07 million). However, this process would be
complicated to operate, would generate awaste byproduct (liquid ammonium chloride) requiring
offsite disposal and would be prone to foulingby
scaling and bacterial growth.The next least
expensive process capable of achieving 98 percent reduction was breakpoint chlorination
($9.73 million). However, this processposes significant safety and site securityconcerns
(chlorine
gas is extremelyhazardous), would significantly increase effluent total dissolved salt (IDS)
concentrations and therefore would increase effluent aquatic toxicity, and could generate chlorinated
organics that could in turnincrease
effluent aquatic toxicity. Lastly, the nextleast expensiveprocess
capable of achieving 98 percent reduction was nitrification of the combined wastestream
as a single
stage process ($11.71 million) or as a tertiary process ($11.41 million). Both processes would result
in an increase in effluent TDS and both processes would provide variable performance based on the
variability of influent bio-inhibiting compounds. At times, neither process would comply with the
requirements of 35
ILL. Admin. Code 304.122a and 304.122b (even those these are not
applicable to
the Noveon-Henry Plant).
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2.11
Evaluation of
Alternative
Methods ofEffluent Ammonia-Nitrogen Measurement
Numerous treatment processes were evaluated to reduce effluent ammonia-nitrogen.
Effluent
ammonia-nitrogen was reduced but with greater difficulty in many cases than expected. This
difficultymade me question whether there could be a fundamental error in the measurement of
effluent ammonia-nitrogen. The method used by the IEPA laboratory andthe outsidelaboratory
used by the Noveon-Henry Plant for effluent compliancemonitoringwere the same. Both
laboratories used the ion selective probe method.This method is recognized by USEPAas
registering artificially elevated values in the presence of organicnitrogen compounds. These
compounds are likely to be present in the Noveon-Henry Plant effluent. Noveon, at my suggestion,
conducted a testing program where the secondary clarifier effluent was analyzed using the historical
method without distillation, the historical method with distillation, andthe phenate method -with
distillation. All threemethods are approved by USEPA. The last method mentioned was the method
least prone to interference by organic nitrogen.
Results of this test method indicated a slightly lower
value for effluent ammonia-nitrogen with distillation andwith the phenate method. However, the
average ofall values was within
15 percent regardless of the method selected. This finding indicated
the historical effluent ammonia-nitrogen concentrations were reasonably accurate and that the
historical method could continue to be used with reasonable accuracy to monitor effluent
ammonia-nitrogen concentrations. The effluent concentrations measured throughout all treatment
evaluations could be considered reasonably accurate. Effluent ammonia-nitrogen reductionhad
indeed been as difficult to achieve as measured.
3.0
OTHER
ISSUES RAISED
BY IEPA
3.1
GAC Treatment of Influent
GAC (granular activated carbon) has been used to remove inhibitors from wastewaters and one of
the inhibitors (possibly the predominateinhibitor) is removable by GAC. So, at face value this
suggestion appears reasonable. However,
several factors render it non-practical. First, the influent
does contain some organics that are readily degradable such as isopropyl alcohol and ethanol. These
readily degradable organics would cause bacteria to grow on the GAC column and slime over the
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GAC pore spaces rendering the GAC unavailable for removal ofinhibitors. Second, the inhibitors
are not the only compounds in the influent that would be adsorbed by the GAC prior to being
slimed
over.
Recall that 5000 mg/L PAC or
17 tons/day was required to prompt nitrification.
Consequently, the GAC usage (evenif sliming were not an issue) would be excessive in the order of
tons/day.
3.2
Implication that
Noveon has not implemented any Ammonia-NitrogenRemoval
Measures
Noveon has installed in-plant recovery devices and instituted pollution prevention plans to minimize
the discharge of organic nitrogen (such as tertiary butyl amine)
to the WWTF
which have been
converted to ammonia-nitrogen through biological treatmenthad such recovery not been provided.
Noveonhas evenbeen recognized by the State of Illinois for progress in pollution prevention
(Annual Govemor’s Award for Pollution Prevention in 1999,2002, and 2003 with Governor’s
Citation Award for Pollution Prevention in 1998). Second, the Noveon-Henry Plant has consistently
removed ammonia-nitrogen through its WWTF as a nutrient required forBOD removal
(approximately 0.04 lbs ammonia-nitrogen removed/lb BOD removed). BOD-removing bacteria
are more tolerantof inhibitors than are nitrifyingbacteria.Without this BOD removal, Noveon
would discharge approximatelyan additional 20 mg/L ammonia-nitrogenin the final effluent. The
Noveonwastewater just contains more ammonia-nitrogen than required as a nutrient for BOD
removal. Lastly, it should be noted that Noveon has exerted significant effort in conducting two
full-scale trials in an attempt to demonstrate a WWTF modification that would provide effluent
ammonia-nitrogen reduction. One trial provided less than a20 percent reduction and the other trial
provided no reduction.
3.3
Attempt to Compare Cost ofAmmonia-Nitrogen Removal between Noveon and
Others
As described in I above, the Noveon-J-lenry Plant has several unique features that render its cost of
providing ammonia-nitrogen removal more expensive than others. The comparisons made by the
JEPA considered only the capital costs of single
stage nitrification. Operations and maintenance
(annual) costs were not included in the comparison.
However, as noted in Exhibit C,
these annual
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costs for Noveon would be significant The
facilities used in the comparisons by the IEPA were
likely required to add little or no chemicals to achieve nitrificationwhereas the Noveon-Henry Plant
would be required to spend $788,000 annually on
chemicals alone. This high chemical costis due to
chemicals required for the pH 2 pretreatmentprocess (acid to lower the pFI and caustic to raise the
pH for biological treatment) and caustic required providing the alkplinity consumed in nitrification.
This yields a present worth chemical only costof $5.29 millionexcluded from the cost comparisons
made by JEPA (based on a 10 year project life). IEPA suggested that a 20 yearproject life would be
more representative. Under this project life, the presentworth cost of chemicals would increase to
$7.73million. Eitherway, this is a significant omissionin cost comparisons. In addition, this does
not include the added operating costthat Noveon would haverelated to pretreatment system
operations andincreased aeration horsepower. Only presentworth costcomparisons are meaningful
when there is a significant difference in operating costs
as is the case here. In my
professional
opinion, thereis no doubt that single stage nitrification at the Noveon-HenryPlant would be far
more expensive on apresentworth basis than any facility the JEPA used in its comparisons.
It is likely that apresentworth cost comparison of these facilities would reveal that the cost of
ammonia-nitrogen
removal is less than $0.20/lb (the surcharge costimposed by the Knoxville
Utility
Board on ammonia-nitrogenis $0.12/pound of ammonia-nitrogen) for the POTWs. The present
worth cost for Noveon to implement
single stage nitrificationis $3.60/lb to $2.32/lb (depending on
whether a 10 year or 20 year project life is assumed,respectively) of ammonia-nitrogen reduced or
18 to
12
times the costfor facilities of the type described by the JEPA.
4.0
INCREMENTAL
COST OF
PROVIDING EFFLUENT AMMONIA-NITROGEN
REDUCTION
The IEPA suggested that they would be more supportive of Noveon’s Petition for Adjusted
Standard ifsome effluent ammonia-nitrogen removal were provided. Itis my professional opinion
that JEPA has failed to recognize that the Noveon-HenryPlant already provides effluent
ammonia-nitrogen reduction through source control practices and ammonia-nitrogen removal
accomplishedin BOD removal. Nevertheless, Noveon requested that Brown and Caidwell calculate
the cost of incrementally providing effluent ammonia-nitrogen reduction. I personally developed the
basis for this cost analysis and reviewed and approved the process by which
theywere calculated. In
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some cases incremental effluent ammonia-nitrogen would be accomplished by treating only a
portionof the wastewater. In other cases, it would be accomplished by sizing the treamient vessel to
only provide partial treatment. The results of this exercise are summarizedin Exhibit D.
These results indicated that even a 25 percent reductionin effluent ammonia-nitrogen would have a
presentworth cost of $1.8 million
to $3.9
million depending upon the treatment process selected.
Moreimportantly, the
25 percent reduction would not
achieve compliance with 35
ILL. Admin.
Code 304.122b assuming it applied and
it
does not apply.
5.0
SUMMARY
The Noveon—Henry Plant currentlyprovides effluent ammonia-nitrogen reduction through source
control and removal associated with BOD removal nutrient requirements. In my professional
opinion, any furtherreduction in effluent ammonia-nitrogen is not required by
35 ILL.Admin.
Code 304.122 ifIEPA approves Noveon’s installationof an effluent diffuser. This diffuser will allow
a more uniform distribution of the effluent from the WW1Pin the Illinois River andwill allow
water quality criteria to be maintained. Both 304.122a and 304.122b do not apply because the
Noveon-Henry Plant clearly has an untreatedwasteload with a population equivalent less than
50,000 based on
all relevant calculations.
Consequently, no effluent limitations and therefore no additional effluent ammonia-nitrogen
reductions are required by this Code.
Extensive efforts have been made by Noveon and its consultants over the last
14 years in examining
effluent ammonia-nitrogen reductions. These extensive improvements
and studies havenot been
taken to seek compliance with 35 ILL. Admin. Code 304.122. They have been undertaken in good
faith to resolvedisputes with the IEPA and to evaluate whether there were any feasible technologies
that would provide additional effluent ammonia-nitrogen reduction.
The
findings of effluent ammonia-nitrogen reduction efforts have been shared with IEPA and are
summarized inExhibits C, D, and E. These findings show the following
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The Noveon-Henry Plant has atleast eight unique characteristics that render it unusually
difficult andexpensive to achieve any further ammonia-nitrogen removal.
Every proven treatment process for effluent ammonia-nitrogen reduction has been
considered by the Noveon-HenryPlant, even onethat was in the developmental stages.
Noveonhas had several consultants evaluate effluent ammonia-nitrogen removal. These
haveincluded awell-respected Illinois firm, a nationally-recognized engineering firm, and a
research professor from England.
No treatment technologywas found by IEPA or anyof these consultants that could provide
significant effluent ammonia-nitrogen reduction (greater than 50 percent) for a present
worth cost of less than $5.0 million. Even a 25 percent effluent ammonia-nitrogen reduction
had apresent worth
cost of at least $1.8
million. Neitherof these removals is required to
comply ‘with 35 ILL. Admin.
Code 304.122a or
304.122b since they are not applicable to the
Noveon-I-lenry Plant.
The present worthcost of installing single stage nitrification, like facilities IEPA used in cost
comparisons, was $11.7 million. This costwhen compared to the surcharge cost imposed by
a POTW on ammonia-nitrogen indicated that the Noveon-Henry Plant costs for
ammonia-nitrogen removal would be
18
times greater than that fora POTW. This cost
difference was not revealed in IEPA analysis due alack of consideration given to
disproportionate operating costs.
In my professional opinion, Noveon has gone far beyond that which Illinois regulations require in
evaluating effluent ammonia-nitrogen removal.
Good
faith and awillingness to work with IEPA
have been demonstrated. Fourteen
years and considerable resources have been applied in effort to
find an agreeable position with IEPA. Such an agreementwas not reached. Noveon’s Petition for
Adjusted Standard is reasonable and should be supported by the Board in conformity with Illinois
regulations.
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CERTIFICATE
OF SERVICE
The
undersigned
certifies
that a
copy of
the
foregoing
Notice
of
Filing
and Written
Expert Testimony
of Houston Flippinwas
filed by
hand
delivery with
the
Clerk
of the
Illinois
Pollution
Control Board
and served upon the
parties
to
whom said Notice
is
directed by
first
class
mail,
postage prepaid, by
depositing
in
the U.S.
Mail
at
191
N. Wacker
Drive,
Chicago,
Illinois
on Friday,
February 6, 2004 and facsimile.
CHO1/12336513.1

m
0~
—1-
±

EXHIBIT A
RESUME
OF T. HOUSTON FLIPPIN, P.E., DEE

Back to top


T.
Houston
Flippin,
P.E.,
DEE
Assignment
Experience
Summary
Capacity Evaluation
Houston Flippin has 20
years
of experience in
industrial and municipal
Education
wastewatermanagement.
Mr. Flippin is particularly adept at maximizing
M.S.,
Environrnenta~
and Water
treatment process
performance.
This is due
to
years
of conducting,
vdftu•~”1984
evaluating,
and
developing
full-scaleprocess design
and operatingguidelines
from bench-, pilot- and
full-scale wastewatertreatment studies. These
E.,
Civ
and Environmental
studies have evaluated both biological
and
physical/chemical processes for
Vanderbilt
University,
1982
treating waters, wastewaters,
and
sludges
laden
with
conventional pollutants,
Registration
priority pollutants,
and
aquatic toxicants.
Mr. Flippin has used
this
Professional
Engineer.
Tennessee,
experience to bothdevelop treatmentcost savings
(capital
and operating)
Illinois, Kentucky, and Michigan
while
maintaining
reliable effluent
compliance and to negotiate more
Diplomate:
American Academy of
reasonable effluent
limits. His
“hands
on”
experience
and his
talent for
Environmental Engineers
communication
has
made
him a
frequent
workshop lecture, client
staff
Experience
trainer, and negotiator.
Recentwork on
the
industrial side has involved
20
years
developing innovative, reliable and cost-effective pretreatment processes
Joined
Firm
and
minimizing upgrade costs of treatmentlagoon systems. Recent work on
1984
the municipal side
has involved rerating capacities of POTWs using site-
Relevant
Expertise
specific data, developing cost saving actions for aeration and sludge
Developing
sfte
specific operating
handling,
and
developing staff reorganization plans to enhance productivity.
guidelines and
treatment
Mr. Flippin
also
has
experience in potable water treatment, stormwater
capacibes.
permitting, wasteload surveys, and waste minimization.
I
Developing cost savings for
________________________________________________________________________________
treatment
plants.
Organic Chemicals, Herbicides and Pesticides
Process Design, Start-up Assistance and Operator Training,
Ciba-
Geigy Corporation
LeadEngineer andAutbor.
Responsible for an on-site
treatability studies,
process design development,
and final report for the treatment of
wastewaters discharged from Ciba-Geigy Corporation’s largest U.S. organic
chemicals manufacturing complex including pesticides. The project began
by evaluatingconversion of the existing aeratedlagoon system to activated
sludge. This conversionwas necessaryto meet effluent requirements under
higher
loading conditions
and
to meet RCRA closure requirements of on-
site surface impoundments.
This
evaluationinvolved
an activated sludge
treatability study evaluatingthe impact of varying totaldissolved solids
concentrations (0.5 percent to 2.5 percent),
temperatures (8°Cto 20°C)
and
RCRA regulated
stream discharge contributions. A process design for the
aerated lagoon/activated sludge
conversionwas developed, presented, and
implemented.
Mr. Flippin developed materials for
and
assisted in the
operator training course which preceded startup of the activated sludge
plant.A follow-up treatability study was conducted
and focused
on
TKN,
TOC, acute
toxicity
and color reduction through the use of PACT®
treatment as
compared to
tertiary
GAC treatment.
Special batch treatability
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T. Houston
Flippin,
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testing evaluated alternative source control methods for a
highly
colored
wastestream. A process design was developed to meet revised treatment
objectives, a final report was issued, and a new WWTF was constructed.
Startup
assistance
and operator
training were provided for
both WWTFs.
Process Design, Rhodia, Mount Pleasant, Tennessee
LeadEngineer andAutbor.
Responsible for an
treatability studies, process
design development, and
final report for the treatment of herbicide
wastewaters. Treatments evaluated impact of
photolytic decomposition,
carbon adsorption,
and
macroreticular resins. Solutionimplemented
included minor treatmentand recycleof waters.
Site converted to a nearly
zero discharge operation.
POTW
Impact and Discharge Negotiations, American Cyanamid,
Barcoloneta, Puerto Rico
LeadEngineer andAutbor.
Responsible for an treatability studies that
evaluated impact of herbicide
and
pesticide wastestreams on
POTW.
Testing indicated no adverse impact on BOD removal, nitrification,
and
sludge
quality
at the desired discharge rates.
Results of testing were used to
negotiate allowed discharges of these wastestreams to the
POTW
without
pretreatment.
WWTF
Troubleshooting, Zeneca Fine Chemicals, Mount Pleasant,
Tennessee
LeadEngineer andAuthor.
Responsible for treatability studies that evaluated
impact ofvarious organicchemical, herbicide and pesticide wastestreams on
site’s biological wastewater treatment facility (WWTF). Developed approach
for screening impact of new wastestreams on the WWTF.
Prescribed
maximum allowabledischarge
rates of each process waststream to prevent
upset of
the WWTF.
Pulp and Paper
Comprehensive WastewaterManagement Plan, Chesapeake
Corporation, West Point, Virginia
Lead Engineer, Field Team Manager,
andAuthor.
Developed a comprehensive
wastewatermanagement plan for a Chesapeake Corporation
1,800
tpd
integrated mill.
Wastewater characterizationstudies defined sources and
distribution ofwaxes through the pulping and paper making process, the
impact of secondary fiber production on
W.’F
solids management, the
impact of bleachingprocess chlorine substitution on influent wasteloads,
effect of separate
and
combined settling of pulp mill and paper mill
wastewaters, and impact of various equalization basin sizes
and
modes of
operation on influent load dampening.
Batch treatability tests evaluated
alternative primary clarification schemes,
alternative site applications of
dissolved
air flotation (DAF) for
wax
removaland solids recovery, impact
of CO2 stripping/coagulation and flocculation on pure oxygen activated
sludge settleability
andimpact ofsecondary fiber on activated sludge settling
properties.
Continuous flow treatability studies evaluated the
effects of
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T. Houston Flippin, P.E.,
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secondary fiber production, secondary fiber wastestream DAF
pretreatment, aeration basin
temperatures, slimicide
loadings and bleaching
plant
chlorine substitution
on pure oxygen activated sludge plant
performance (particularly
sludge
settleability).
The continuous flow
treatability studies also involved evaluation of several types
of biological
selectors to control filamentous sludge
bulldn~aerobic, two-stage aerobic,
anoxic/anaerobic, and extended anoxic/anaerobic.
Elements of
this project
were presented by Mr. Flippin atthe
1992 TAPPI Environmental
Conference.
Lagoon Modeling and Upgrade Evaluation, Confidential Client,
Midwest
LeadEngineer.
Developed alternative upgrade measures
for a wastewater
treatment lagoon systemto accommodate increased wasteload
while
not
exhibiting H2S emissions.
One alternative was based
on operatingthe
lagoons without oxygen
and nutrient deficiencies and thus
achieving greater
BOD removal rates.
This alternative was based on treatability
data.
The
second alternative was based on operating the lagoons under oxygen and
nutrient limitations,
which decreased
BOD
removal rates but minimized
upgrade requirements.
Extensive
full-scale
system data was used to develop
a
model
for
evaluating
system performance under altemative conditions.
The project is currently
in the
final design stage.
Hazardous Waste
Groundwater Remediation Process Design, FLTG, Incorporated,
Crosby, Texas
P?vjectManager and LeadEngineer.
Responsible for a groundwater
remediation project for a company formed by 80 principle
responsible
parties.
This Superfund site groundwater treatability investigation
considered how bestto
upgrade the
existing treatment
facility.
Air
stripping, peroxidation,
ozonation, ultrafiltration,
carbon
adsorption, resin
adsorption,
and anaerobic degradationseparately and in conjunction with
activated sludge treatment were considered.
Following a series of batch and
continuous
flow treatability tests, activated sludge treatment followed by
granular activated carbon treatmentwas selected as the most cost-effective
means of
achieving discharge targets.
In addition, a cost-effective sludge
treatment and disposal planwere developed.
Textiles
Toxicity Reduction Evaluation/Toxicity Identification
Evaluation,
Globe Manufacturing, Gastonia, North Carolina
Prefect
Manager, Lead Engineer,
andAutbor.
Managed a wastewater
pretreatment project where the
industrial
discharge was cited
as the source
ofthe POTW’s
effluent aquatictoxicity problem.
Treatability tests were
conducted which screened the
effects of the
following treatment processes
on effluent toxicity reduction:
air
stripping, cation exchange resin,
activated
silica, macroreticular
resin,
granular
activated carbon, and biohydrolysis.
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T.
Houston
Flippin, P.E.,
DEE
Results of these tests
and further
desktop evaluations indicated the
biotoxicant was ethylene diamine and that activated sludge treatment would
provide the most cost-effective treatment.
Continuous flow treatability
studies were used to develop the process design
for the selected process.
Submitted
design basis report for the pretreatment facility, reviewed final
design drawings and specifications, and provided
startupassistance.
The
pretreatment facility eliminated all acute
and chronic toxicity
associated
with
the wastestream discharge at its flow contribution to the POTW.
Elements
of this projectwere published in
Water Science Technology,
Volume 29, No. 9
(1994).
Food Processing
Waste Minimization, Quaker Oats, Newport, Tennessee
Project
Manager, LeadEngineer,
andAutbor.
Developed a waste minimization
plan for a Quaker Oats
facility.
On-site wastewater characterization studies
coupled withinterview of site personnelwere used to develop practical,
cost-effective waste minimization recommendations.
Implementation of
the plan resulted in significant reduction of product losses and sewer
pretreatment surcharges.
Combined Municipal/Industrial Wastewater Management
ISP Chemicals, Calvert City, Kentucky
Principa/Engineer/Site CSM:
Investigation of theimpact of eightwaste
streams on the
onsite activated sludge process.
Clariant
Corporation,
Elgin, South Carolina
Provided alternative treatment system analyses prior to the
construction of a
Greenfield wastewatertreatment
facility.
Cooperative and Cost Effective Wastewater Treatment,
Ryan
Foods
Company, Murray, Kentucky
Project
Manager
and
PrincipalEngineer.
Worked with City of Murrayand
industry to developa
“win-win”
strategy
for minimizing wastewater
treatment costs for
both
the City
and industry.
Early estimates by the
City’s
consultant
had indicated that the
POTW
would have to spend
approximately $10 million to accommodate the discharge wasteload on the
POTW with
Ryan Foods at maximum loading
(and without pretreatment).
Estimates indicated that Ryan Foods would have to spend $3
million to
meet the
limits
requested
by the Cityifpretreatment were to be installed.
A
review of pertinent information indicated the opportunity for significant
savings byboth parties.
Treatability
studies were conducted
and POTW
performance data were reviewed.
This
work indicated that a much less
costly approach could be taken.
A final design was developed for the
pretreatment facility and installed
at a cost of $1.6
million.
The
pretreatment facility reduced the wasteload
by approximately7O percent.
However, the remaining wasteload to the POTW exceeded the “rated
capacity” of the POTW.
A site-specific analysis was conducted
and
used to
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T.
Houston Flippin,
P.E., DEE
rerate the capacity of the
POTW.
A
major component of this
analysis
was
sludge stabilization and alternative disposal methods.
This
rerating allowed
the POTW
to gain an
additional 29 percent
in rated capacity for a cost of
$0.7
million. So, in the end, the City
of
Murray
and Ryan Foods both saved
more than
$1
million
each.
The City
also
received definition
ofalternative
sludge
disposalmethods and a description of the incremental upgrades
that
would be required in the future as the
“real ratedcapacity” of the POTW
was approached.
Municipal Wastewater Management
Change Management Program, Metro Water Services, Nashville,
Tennessee
Assistant
Task
Managerfor Operations Grv4.
Worked with client to identify
cost-saving
action items to reduce annual
O&M costs at
two
water
treatmentplants
and
three wastewater treatment plants.
The purpose in
these reductions was to render the plants’
operating
costs competitive with
that estimated by private contractors and thus “stave off privatization.”
Annual savings of greater
than
$1,000,000 were identified.
Currently
serving
as advisor to
teams
implementing savings
regarding
sludge
thickening
and
dewateringand
aeration.
In addition to
this
work, have
assisted client in process troubleshootingwhich has allowed client to avoid
effluent non-compliance.
0etrochemical and Synthetic
Fuels
Safety Kleen Corporation, East Chicago, Indiana
Lead Engineer,
Project
Manager, andAuthor.
Responsible foron-site
wastewater treatment
facility (WWTF) process troubleshooting and
training
to facilitate
compliance with pretreatmentlimits
at this
facility, one
of the
largest oil re-refineries in the world.
Treatability studies and process design
were required for
WWTF
modifications to accommodate increased
production and more
stringent pretreatment limits.
Brown
and Caldwell provided sampling and analytical
procedures modified
for cyanide, ammonia,
and
orthophosphate analyses.
A more
comprehensive and site-specific procedurewas implemented to evaluate the
chemical conditioning requirements of the mixed liquor. “In situ” oxygen
transfer was determined to assess upgrade requirements.
Treatability studies were conducted. The effects of operating temperature
(30°Cto 60°~
and F/M ratio
(0.1 lb COD/lb MLVSS
day to 0.7 lb
COD/lb MLVSS
day) on activated sludge
settleability
and effluent
quality
were evaluated.
The effects of
steam
stripping,
as a pretreatment step, on
activated
sludge systemperformance were evaluated.
Metals precipitation
with
lime, alum and
caustic was studied as a pretreatment and post
treatment process.
High pH air stripping
and
breakpoint chlorination were
examined as
effluent NH3-N reduction technologies.
Effluent peroxidation
and ozonation were evaluated as
a means of providing effluent total
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T. Houston Flippin,
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phenolics reduction.
The use of a biological selector and chemical
conditioning
(e.g., coagulation and flocculation) were investigated as means
of improving sludge
settleability.
A process design to upgrade the existing WWTF was provided and included
a four stage, aerobic biological selector,
temperature and pH
control,
coagulation, flocculation, increased RAS
pumping capacity, breakpoint
chlorination and tertiary filtration.
Final design guidance
was provided on
selection of equipment forthe
biological selector and
tertiary
filtration.
Booth Oil Company, Buffalo, New York
Lead Engineer andAutbor.
Responsible for wastewatersampling program to
define
treatmentprocess limitations under increased future loading
conditions.
Treatability testing was
conducted to evaluate alternatives for
controlling total phenolics discharge. Both improvements
in oil/water
separation and hydrogenperoxide treatment were considered.
A report
presenting
alternatives for upgrading WWTF
operations and for
prioritizing capital improvements was presented.
Groundwater Remediation Process Design, FLTG, Incorporated,
Crosby, Texas
Project
Manager andLeadEngineer.
Responsible for a groundwater
remediation project for a companyformed
by 80 principle responsible
parties
(almost exclusively petrochemical industries and refineries). The
groundwater at
this
siteexhibited
an influent COD of approximately 600
mg/L and had free product present. A groundwater treatability investigation
was conducted to determinehow best
to upgrade the
existingtreatment
facility.
Air stripping, peroxidation, ozonation,
ultrafiltration, carbon
adsorption, resin adsorption, and anaerobic degradation separately
and
in
conjunction with activated sludge treatment were considered.
Following a
series of batch and continuous flow treatability tests, activated
sludge
treatment
followed
by granular activated carbon treatment was selected as
the most
cost-effective means of achieving discharge targets.
In addition, a
cost-effective sludge
treatment and disposalplan were developed.
Reilly
Industries, Lone Star, .Texas
LeadEngineer, ProjectManagerandAutbor.
Responsible for a two-tiered
project at
this coal
tar plant. Treatability studies were conducted and
process designs
were developed for alternative wastewater treatment facility
upgrades that would allow plant to meet more restrictivepretreatment
limits. A
work plan was developed
in cooperation with TNRCC that would
allow
the POTWto seek permit reliefwhich in turn would
allow the plant
to not require
WWTF
upgrades.
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T. Houston Flippin, P.E., DEE
Permitting
Hunt Foods (formerly Quaker Oats), Newport, Tennessee
Project Manager
and
Principa/Engineer
on project involving wasteload
minimization, pretreatment facility design and negotiation of pretreatment
limits.
Laidlaw (formerly Osco, lnc), Nashville, Tennessee
Project Manager andPrincipalEngineer
on project involving pretreatment
facility
design, startup, troubleshooting, and pretreatment permit negotiations.
J. Hungerford Smith, Humboldt, Tennessee
PrincipalEngineeron
project involving pretreatment facility
design, POTW
upgrade
design, and pretreatment permit negotiations.
Ryan Foods Company, Murray,
Kentucky
ProjectManager
and
PtincipalEngineer
on project involving pretreatment
facility design, construction management, startup, operator training, POTW
upgrades, pretreatment permit negotiations, and negotiation ofre-rated
capacity of POTWwith Kentucky Division ofWater.
BF Goodrich Performance Materials,
Henry,
Illinois
Project Managerand PrincipalEngineer
on projectinvolving treatment
facility
design,
startup,
operator training, treatment facility troubleshooting and
NPDES permit negotiations withIllinois EPA. Meeting withIllinois Water
Pollution Control Board is pending.
ISP Chemicals, Texas City, Texas
ProjectManager and PrincipalEngineer
on project
involving modifying existing
NPDES permits
for stormwater
and
wastewater. Project also involved
conduct of testingto get adjusted metals limits.
OxyVinyls (formerly Geon Canada), Niagara Falls, Ontario,
Canada
ProjectManager and PrincipalEngineer
on projectinvolving treatment
facility
troubleshooting, operator training, and “NPDES equivalent” permit
negotiations.
Confidential Client, Barceloneta, Puerto Rico
Project Managerand Principa/Engineer
on project involving treatability testing
and pretreatment permit negotiations.
Toxicity Reduction
Thiokol Corporation, Brigham City, Utah
LeadEngineer
on effluent toxicity identification evaluation
(TIE)
followed by
toxicity reduction evaluation (TRE) as
a part of treatability studies fora
newly designed
WWTF.
The new WWTF replaced two existing
WWTFs
that were abandoned.
Acidification, air stripping, alkalinization, chemical
P.’~flOJ~23417
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T. Houston
Flippin, P.E., DEE
reductionwith sodium thiosulfate, filtration, granular activated carbon, ion
exchange (anion and cation), macroreticular resin, and metal complexing
with EDTA, were evaluated as a
means of achieving effluent toxicity
reduction for a selected wastestream.
High salinity was identified as the
toxicant.
The client decided to blend the
selected wastestream with other
wastestreams causing a decrease in wastewater salinity and an increase in
wastewaterBOD.
Activated sludge treatment followed by ozonation
as
a
means of toxicity reduction and disinfection was determined toprovide
consistent compliance
with
effluent BOD and toxicity limits.
A process
design was provided.
The newly designed WWTFs included gritremoval,
equalization, activated
sludge treatment, granular media filtration and
ozonation.
The final
design for the WWTF was reviewed for consistency
with the process design.
Confidential Client, Indiana
LeadEngineer and Project EngineerA
Toxicity Identification
Evaluation
(TIE)
was
conducted for a large-volume producer
of metal ingots and sheet
aluminum.
The TIE used Phase I laboratory characterization procedures,
single
stream toxicity testing, and resynthesis testing with major
wastestreams treated for
toxicity
removal.
Both
Ceriodapbnia
and the fathead
minnow were used in acute tests
throughout the study.
Study results
indicated that adsorptive organic compounds
associated with an internal
waste treatmentprocess were primarily
responsible
for
toxicity.
Pure
chemical
testswith
the
wastewater treatmentpolymer used at
the
site
indicated that the
polymer
may play a role in effluent toxicity.
A Toxicity Reduction Evaluation
(TRE) work plan was
also conducted for
the client to developa means to cost-effectively reduce
effluent
toxicity as
required by the
State.
Services includedwasteload characterization and
wastewater treatment
facility (WWTF)
optimization.
Memberships
National Society of Professional Engineers (NSPE)
Technical Associationof the Pulp and Paper Industry (TAPPI)
Water Quality Committee Member
Water Environment Federation
Pretreatment Committee Member
Chi Epsilon
-
National Civil Engineering Honor Society
Publications/Presentations
~Enhanced
Activated Sludge Treatment of High Strength Bio-inhibitory Industrial Wastewater’ with
R.
Rhoades,
10th
Annual WEF
Industrial Wastes Technical and Regulatoiy Conference,
Philadelphia, Pennsylvania, August 2004.
‘Treatment Alternatives for Removing Ammonia-Nitrogen from Landfill Leachate’ with RE. Ash and
B.N. Card, Annual Tennessee Solid and Hazardous Waste Conference, Gatiinburg,
Tennessee,
April2004.
‘Alternative
Considerations inSizing Aeration Basins
with W. W.
Eckenfelder, Design,
Performance and Operation of Biological Treatment Processes Pre-Conference Workshop,
VanderbiltUniversity and USEPA Conference, ‘Industrial Wastewater and Best Available
Treatment Technologies: Performance, Reliability, and Economics”,
Nashville, Tennessee,
February
2003.
P~\PROJ\23417
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8
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T. Houston Flippin, RE., DEE
‘Modifying Equalization to Provide Pretreatment of High Strength Wastewaters” with D.A. Moye,
19th Annual
North Carolina AWWMNEF Conference Proceedings,
Winston-Salem, North
Carolina,
November 2002.
‘Benefits of Using Nitrate as Nutrient in Activated Sludge Treatment Systems’ with W.
W.
Eckenfelder and D,A. Moye,
8th Annual WEF
Industrial Wastes Technical and Regulatory
Conference, Atlantic City, New Jersey, August2002.
‘Biological Treatment of High TDS Wastewaters,” with W. W. Eckenfelder and V. J. Boero, Water
Environment Federation-Industrial Waste Technical and Regulatory Conference, Charleston,
South
Carolina,
August 2001.
‘Competitive Performance for Water and WastewaterUtilities,’ with J.L
Pintenich, Nashville Quality
Forum, Nashville,
Tennessee, October 1999.
‘Reclaiming P01W Capacity,’ with M.L.
Roeder, American Society of Civil Engineers-Tennessee
Sectlon Annual
Meeting, Nashville,
Tennessee,
October1999.
‘Batch Activated Sludge Testing to Determine The Impact ofIndustrial Discharges-orrPOTW
Performance’, with J.S. Allen,
Proceedings of
1998 WEFIndustrial Wastes Specially
Conference,
Nashville, Tennessee,
March 1998.
‘Economics of Treating Poorly Degradable Wastewaters in the Chemical Industry,” with
KD. Torrens,
Proceedings of1998 WEF Industrial Wastes
Specialty
Conference,
Nashville,
Tennessee, March 1998.
‘Effects of Elevated Temperature
on the Activated Sludge Process,’ with W.W. Eckenfelder, Jr.,
Proceedingsof 1994 TAPPI lntemationalEnvironmental Conference,
Portland, Oregon,
April
1994.
‘Toxicity
Identification and Reduction in the Primary Metals Industry,’ presented at
Spring AIChE
Conference,
Atlanta, Georgia, April
1994.
“Treatability
Studies and Process Design for Toxicity Reduction for a Synthetic Fiber Plant,~with
J.L.
Musterman,
WaterScience Technology,
Vol. 29, No. 9(1994).
“Granular Carbon Adsorption of Toxics,’ technical reviewof chapter four in
Toxicity Reduction in
Industrial Effluents,
P. W. Lankford and W. W. Eckenfelder,
Jr.
(Eds), Van Nostrand Reinhold,
1992.
“Diagnosing and Solving a Pulp
and Paper Mill’s Poor Activated Sludge Settleability Problems
Through Treatability Studies,’with M. A. Bellanca,
Proceedings
of
1992 TAPPI Environmental
Conference,
Richmond, Vii~inia,1992.
‘Hydrogen Peroxide Pretreatment of Inhibitory Wastestream
Bench Scale Treatability Testing to
Full Scale Implementation:
A Case History,’ with R.
L. Linneman,
Proceedings ofChemical
Oxidation:
Technologyfor 1990’s,
Vanderbift University, Nashville,
Tennessee,
1991.
‘Control of Sludge Bulking in a Carbohydrate Wastewater Using a Biosorption
Contactor,”
with
W. W.
Eckenfelder, Jr.
and M. A. Goronszy,
Proceedings ofthe 39th Annual Purdue Industrial
Waste
Conference,
1984.
Research Topics
Biodegradation of PCB5 and HCB, research conducted at ECKENFELDER
INC.
Volatile Organic Compound Emissions from Activated
Sludge Systems,
research conducted at
ECKENFELDER INC.
Performance of Selective Bacteria in Industrial Activated
Sludge Systems,
research conducted at
Vanderbilt University
Biosorption for Improved Reactor Capacity, research conducted at Vanderbiit Univers+ty
Control ofActivated Sludge Bulking Through the Use of a Biosorption Contactor,
research
conducted at Vanderbilt University
Workshops
Instructor, Tennessee State University,
“Monitoring
Requirements, Operating Guidelines,
Calculations, and Troubleshooting,’ presented during ‘Aerobic Biological Wastewater Treatment
Workshop,’
Nashville,
Tennessee,
November1997, April 1998,
November1998,
and April
1999.
N
Instructor, Mississippi Water Pollution Control Operators’ Association, Inc., ‘Clarifier Operation and
Maintenance Workshop,’ Tunica, Mississippi, April
1997.
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resumo.d~

T.
Houston
Flippin, P.E.,
DEE
Instructor, Brown and Caldwell, ‘Activated Sludge Wastewater Treatment Workshop, ‘attended
by
participantsfrom over
3 municipalities
and 10 industries, Nashville, Tennessee,
November 1999,
March 2000,
May 2001,
November
2002,
and November
2003.
Instructor, Tulane University and Louisiana Chemical Association, ‘Wastewater Strategies for
Industrial Compliance: Gulf Coast Issues and Solutions’, New Orleans,
Louisiana, December 2003.
Honors
Who’s Who of Citation’s Environmental Registry, 1991
Eckenfelder Inc. Technical Employee ofthe Year Award,
1990
Outstanding Young Men of America,
1986
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m
:5-
—÷
oJ

EXHIBIT B
PERTINENT ARTICLES FROMLITERATURE
REVIEW

r
NATIONAL
CORN
L~
HANDBOOK
~
CROP FERTILIZATION
Nitrification Inhibitors for Corn Production
D.
W.
Nelson, University ofNebraska
D. Huber, Purdue University
Reviewers
K. D.
Frank, Univesrity ofNebraska
G. W.
Randall, University of Minnesota
R.
G. Hoeft,
Universityofillinois
W. I. Segars, University of Georgia
D. R. Keeney, University of Wisconsin
J.
T~Touchton, Auburn University
G.
L. Malzer,
Universityof Minnesota
L. F
Welch, University ofIllinois (retired)
H. F Reetz, Jr., Potash & Phosphorus Institute, Illinois
Nitrogen (N) is an essential element for plant
growth and reproduction. The amounts of N taken
up
by corn
exceed
those of any other soil-derived
element. Today an average
25
of plant-available N
in soils
(ammonium and nitrate) originates from the
decomposition (mineralization) of organic
N
compounds in humus, plant and animal residues, and
organic fertilizers, 5
from
N in rainfall, and 70
from
applied inorganic
N fertilizers
(Figure 1). In soils,
organic N
is converted to ammonium through
microbial
decomposition. Ammonium formed in soil,
added as fertilizer, or in precipitation is rapidly
oxidized to nitrate in the nitrification process carried
out by specific bacteria.
Nitrification results in the
production of nitrate, a
form of plant-available N which
is readily lost from soils. Nitrification inhibitors are
chemicals that slow down ordelay the nitriflcation
process, thereby decreasing the possibility that large
losses of nitratewill occur before the fertilizer nitrogen
is taken
up by plants. This publication discusses
N
losses from soils, characteristics of nitrification
inhibitors, and how nitrification inhibitors can
be used
to improve efficiency of corn
production.
THE NITRIFICATION PROCESS
Ammonium (NH4) added to soils or formed
by
decomposition of organic N compounds is oxidized to
nitrite (NO2)
by
Nitrosomonas
bacteria, and nitrite is
further oxidized to nitrate
(NO3) by
Nitrobacter
bacteria in
a process termed nitrification (Figure 1).
Nitrate is normally the form of N taken up by plants;
however, most plants can also assimilate amrrionium.
In
most soils, nitrification of applied ammonium is
rapid
(2-3 weeks), but nitrification rates are greatly
IOWA
STATE
UNIVERSITY
University Extension
NCI-I-55
reduced by cool soil temperature (50°F),low pH
(5.5),
and waterlogged conditions. Nitrification converts
ammonium,
a
positively charged ion that is bound to
clay and organic
matter, to nitrite and nitrate,
negatively charged ions
that arefree in the soil
solution and
are readily lost from the plant rooting
zone of soils.
N
LOSS FROM SOILS
Only about 50
of the applied
N is taken up by
corn
during the year following fertilizer addition. About
25
is immobilized during residue
decomposition or
remains
in the soil as nitrate. The remaining 25
is
lost from the plant rooting zone by leaching and/or
dentrification.
(See Table I for a generalized estimate
of the fate of fertilizer N added to soils.) Some of the
immobilized
N will be
mineralized (5
peryear) and
will be available to subsequent crops. Nitrate
remaining
In the profile at the end of the cropping
season will be
available to the succeeding crop unless
lost over the winter and spring by leaching or
dentrification.
Leaching is important in coarse-textured soils.
Nitrate may be leached from
naturally well-drained or
tile-drained soils
by percolating water. One inch of
infiltrating water will
move nitrate
I
to 2.5
inches
downward in clay loam and sandy soils, respectively.
Thus, during periods of excess
rainfall, leaching may
move nitrate out of the effective rooting zone of
plants.
Denitrification (the microbiological conversion
of
nitrate and nitriteto gaseous forms of N) is the major
pathway of N loss from most fine-textured soils.
It
normally
occurs in
soils
that become
waterlogged by
NCH 55
Revised
February 1992
Electronic version July
20C1

Figure
1. The nitrogen cycle in soils (adapted from Nitrogen in Agricultural Soils).
excessive rainfall or irrigation.
Denitrification occurs at
maximum rates when soils
arewarm (60°F),pH
values
are high (7),
nitrate isplentiful, and an energy source
(carbon) is available.
In waterlogged soils,
more than
100
lb. of nitrate N per acre can
be denitrified within a
5-day period. However,
in cold
soils (40°F)or soils
with low pH values (5), denitrification rates are slow.
TYPES AND USES OF
NITRIFICATION INHIBITORS
Nitrification
inhibitors
(NI)
are chemicals that
reduce the rate
at which ammonium is converted to
nitrate by killing or interfering with the metabolism of
Nitrosomonas
bacteria
(Figure 1). The loss of N from
the rooting zone can
be minimized by maintaining
applied
N in the ammonium form during periods of
excess rainfall
prior to
rapid N uptake by crops. A
numberof compounds have been shown to
inhibit
nitrification in laboratory and field
studies (Table 2);
however, only N-Serve® and Dwell® have U.S.
Environmental
Protection Agency approval foruse
on
cropland in the United States. Additional compounds
are used in Japan and other countries; and
registration isexpected for additional compounds in
the U.S.
N-Serve iscurrently
labeled forcorn, sorghum,
wheat,
cotton,
rice, and
other crops and is sold
in
emulsifiable
and nonemulsifiable formulations. Dwell
was registered as
a nitrification inhibitor
in 1982,
but it
is uncertain
if the product will be
marketed. Both
chemicals are effectivenitrification inhibitors when
Table 1. GeneralIzed
Fate
Applied
to Corn.1
of Fertilizer Nitrogen
Soil texture
Fate of applied
N
coarse
medium
and fine
Plant uptake (first year)
-—
of applied N—---
40-60
50
-
60
Remains In soil as organic
20 -25
25- 30
and
inorganic N
Lost from root zone:
Denitrificatlon
5
-
10
15 -25
Leaching
15-20
0-10
I
Average values over years for soils
in the Combelt and
southeastern
U.S. and irrigated soils of the Great Plains and
western valleys.
0.5 lb. of active ingredient (a.i.)
peracre is used in
a
band application with anhydrous ammonia or N
solution fertilizers.
N-Serve and Dwellmay also
be impregnated on
solid fertilizers or mixed with
N solution fertilizers prior
to broadcast applications.
However, incorporation of
the nitrification inhibitor-treated fertilizer must occur
shortly after application because
both compounds are
volatile.
Higher rates
(2
to
4 times
band applications)
of N-Serve and Dwell are often required to control
nitrification of broadcastammoniacal fertilizers.
Recent studies have shown that NI
can
also be
effectively used with liquid animal
manures and
sewage
sludges
that are injected
into
the soil.
ATMOSPHERIC
GASES
N2, NO2,
N20,
NO
A
A
A
ri
I
NITROGEN
I
FERTILIZER
I
I
/
/
/
#5
V
LEACHINGTO
GROUNDWATER
OR TILE DRAINS
2

Table 2. Compounds Marketed or Proposed as
Nitrification
Inhibitors.
Common or
Registered in
Chemical name
trade name
Manufacturer
the U.S.A.
EFFECTS OF NITRIFICATION INHIBITORS
A number of studies throughout the
United States
have demonstrated that NI
effectively retards the
conversion of ammonlum
to nitrate
in a variety of
soils.
Results indicate that application of NI
delays the
conversion of ammonium to
nitrate for 4 to
10 weeks,
depending upon soil
pH
and temperature. With fall
applications of N fertilizers, NI
minimize nitrification
until low soil temperatures (40°F)stop the process.
With
spring applications,
NI prevent the formation of
nitrate during the late spring when rainfall is high and
uptake of N by crops Is low.
Corn yields are often increased
as
N losses from
soils are reduced by the application of NI
with both
conventional tillage and reduced tillage systems
(Table 3). The potential benefit from
NI application
depends
on a
number of site-specific factors, such as
soil type, climate, cultural practices,
and N
management program. Highest probability of yield
response from NI
occurs with excessively drained or
poorlydrained soils because
of N losses from
leaching and denitrification, respectively. For example,
a study in Indiana with faIl-applied anhydrous
ammonia showedthat
N-Serve application increased
corn yields by 300
with
a very poorly drained silty
clay soil and
1
with
a well-drained sandy loam soil.
Significant corn yield responses from NI additioti have
also been observed with irrigated sandy soils
(Table
4). Yield responses from
NI
are more frequent
with fall
N applications than with spring applications
because of lower N losses from denitrificatlon
normally experienced when fertilizers
are applied
nearer to
the timeof crop
need. There have been
consistent yield responses from NI added to
ammoniacal fertilizers forcorn produced with a
no-till
system, presumably because of larger N losses from
denitrification normally experienced with this
production
method.
The Increased availability of inorganic N and the
presence of ammonium in the soil resulting from NI
addition also
have been shown to increase the protein
concentration of corn grain
(Table 5). The feeding
value of corn increases as the protein level increases.
The application of NI to inorganic and organic N
fertilizers also
has reduced the severity of
Diplodia
and
Gibberella
stalk rots of corn,
likely because of
altered
N metabolism in plants assimilating the
ammonium form of N (Table 6). Cornstalks in areas
receiving NI-treated fertilizers tend
to remain green
later in the growing season and havethicker rinds,
both of which
reduce pathogen effects
and
lodging.
Grain moisture
content at harvest is unaffected by NI
addition to fertilizers.
The amounts
of nitrate leached Into groundwater
and ozone-destroying nitrous oxide
(N20)
emitted into
the atmosphere through denitrification are reduced
by
NI
application. The
use of NI
also gives greatflexibility
in timing the application of N fertilizers. For example,
with most Cornbelt soils
all of the
N
needed for a corn
crop can
be applied
as anhydrous ammonia during
Produced
commercially:
2-chloro.6-(t,ichloromethyl)-pyridlne
5-ethoxy-3-trichloromethyl-1, 2. 4-thiadiazol
Dicyandiamide
2-amino-4-chloro-6-methyl-pyrimidine
2-mercapto-benzothiazole
2-sulfanilamidothiazole
Thiourea
Dow Chemical Co.
Uniroyal Chemical
N-Serve
Dwell, Terrazole
(etradiazol)
DCD
AM
MBT
ST
lU
Yes
Yes
SKW Trostberg AG
Mitsui Toatsu
Co.
Onodo Chemical
Industries
Mitsui Toatsu Co.
Nitto Ryuso
No
No
No
No
No
Proposed as nitriflcation
inhibitors:
2,4-diamino-6-trichloromethyl-5-triazine
Polyetherionophores
4-amino-I, 2, 4-trlazole
3-rnercapto-1, 2, 4-triazole
Potassium azide
Carbon bisulfide
Sodium trithiocarbonate
Ammonlum dithiocarbamate
2, 3, dihydro-2, 2-dlmethyt-7-benzofuranol
methyl-carbamate
N-(2, 6-dimethylphenyl)-N-(Methoxyacetyl)-
alanine
methyl ester
Ammonium thiosulfate
1-hydroxypyrazole
2-methylpyrazole-1 -carboxamide
Amer. Cyanamid Co.
Amer. Cyanamid
Co.
Ishihara
Industries
Nippon Gas
Indus.
Plttsb. Plate Glass Co.
Imperial Chem.
Indus.
Imperial Chem.
Indus.
FMC
FMC
Furadan
(carbofuran)
No
No
No
No
No
No
No
No
No
No
Olin Corp.
CMP
BASF
GOR
No
No
No
3

the previous fall if a NI is
used, thereby reducing the
workload in the critical
spring
planting season. The
use of NI
permits early spring application of N
in many
areas of the United States where N losses are
a
consistent problem.
Data in Table
3 show that
NI addition does not
result in yield increases in
all soils and climatic
conditions.
In
fact, in some situations there is a low
probability of a
corn yield increase from NI.
Since the
purpose of NI
application is
to
increase the
efficiency
and amount of N available to plants by reducing N
losses, no response to NI
will be obtained
during
seasons
orwith soil types having little orno
N
loss.
Little orno
N loss occurs during seasons with below
average rainfall following
N
application because
N
loss through leaching and denitrificatlon is directly
related to the amount and distribution of rainfall and
the drainage characteristics of the soil.
No yield response will be obtained from NI
addition when
N
rates
used are far in excess of those
required for maximum
yield. For example, if maximum
corn
yields could be obtained with 150 pounds of N
per acre but 300 pounds per acre are applied,
as
much as one-half of the applied
N could be
lost before
a decrease in yield occurs. Late side-dress
injections
of N may reduce yield through mechanical damage to
the root system and increased root rot.
Immobilization
of late-season applied
N with a
NI may further
exacerbate this condition.
In sandy soils with very low cation exchange
capacities,
the addition of NI to ammoniacalfertilizers
may not reduce N
loss or increase crop yield because
of differential movement of ammonia and NI from
the
zone of placement. Some
studies have shown that
ammonium ions were leached below the NI treated
zone by rainfall and irrigation
water. In this situation,
nitrification deeper in the profile
produced nitrate that
was subsequently removedfrom the rooting zone by
leaching.
N rate
Nitrlflcatlon InhibItor
None
N-Serve
Dwell
lb/acre
---—-corn yield, bu/acre——-
0
59
60
89
119
98
120
105
151
145
180
136
170
171
240
171
182
186
N applied
Treatment
NH3
NH3
+
N Serve
Iblacre
—grain
protein,
0
6.76
60
7.76
9.24
120
9.38
10.60
180
10.80
11.71
I
Study conducted In Indiana using 373
x Mo 17
corn hybrid.
Table 6.
Effects of a Nitrification Inhibitor on Stalk Rot
of Corn.1
No. of
studies
N
source
Treatment
N
N
+
N Serve
—----
plants with stalk roV------
3
NH3
38
16
4
Swine manure
54
23
1
Average values for all locatIons, years, and
N rates from
studies In Indiana.
Table 5. Effect of a Nitrlflcation InhIbitor on Corn
Grain Protein Concentration.1
Table 3. Effects on Grain Yields of Corn Grown with
Conventional and No-Till Systems
cation Inhibitors to Fall- and SprIng-Applied Ammoniacal Fertilizers.’
frem-Addition-of-Nit-r-ifl~
~
Time
of
No. of
No. of yield
Yield Increase
LocatIon
applicatIon
experiments
increases from NI2
from NI3
Indiana
FaIl
24
17
12.5
Spring
51
29
5.8
Spring (no-till)
12
9
10.0
No. Illinois
FaIl
12
5
5.0
Spring
14
2
So.
Illinois
Fall (NH3)
7
7
Spring (NH3)
9
7
Spring (no-till)
2
2
-1.0
4.6
4.6
8.5
Fall (N solution)
5
4
Spring (N solution)
5
2
3.3
-12
Kentucky
Spring (no-till)
8
7
14.3
Wisconsin
Fall
2
1
4.7
Spring
2
0
1.5
‘Adapted from
R. 0. Hoeft 1984. Current status of nitrification
InhibItors.
In R. O~Hauck(ed.)
Nitrogen
in
Crop Production. Am.
Soc. of
Agronomy, Madison, WI,
2
Significant at 95
probabilIty level.
3
percent yield Increase across all
N rates and locations.
Table 4.
Effects of Nltrificatlon Inhibitors onthe YIeld
of Irrigated Corn Fertilized with
Urea. (Hubbard
Loamy Sand).1
Taken
from 0. L. Maizer,
T.
J. Graft, and
J.
Lensing.
1979.
Influence of nItrogen rate, timing of nitrogen applIcation and
use
of nitrificatlon
Inhibitors for Irrigated
spring wheat
and corn.
In
Univ. Mlnn.
Soil Series 105
Report
on
Field Research In Soils.
4

WHERE SHOULD
NITRIFICATION INHIBITORS BE USED?
The response ofcorn to applications of NI with
ammoniacal fertilizers varies greatly
throughout the
United States
because of major differences in
N loss
potential from differing
climate,
soils, and production
systems.A
summary of research results
on corn yield
responses from NI additionfor
various corn
production regions is
presented
in Table 7, and the
probabilities for obtaining a yield response from NI for
several combinations of region, soil texture, and time
of fertilizer application
are given
in Table 8. The
addition of NI to fertilizer should
be looked upon
as
Insurance against N loss, and, thus, a decision to
use
NI should be
based on
the probability of
obtaining
yield increases
over a
period oftime,
e.g., 5
years.
The usefulness of NI forcorn production in three
general regions of the United States is discussed
below.
Southeast
The response ofcorn to NI applications in the
southeastern United States has been
mixed. The
relatively high soil temperatures during the winter
result In nitrification of fall-applied N and subsequent
leaching or denitrification of the nitrate that is formed.
The
addition
of NI
does not alleviate this problem
becauseof the limited longevity of thecurrently
registered inhibitor compounds in soil
and the long
period of time between N application and crop
uptake
of the nutrient. Thus, yield responses to
NI added to
fall-applied fertilizers
have not been
consistently
observed. A number of studies have shown modest
corn yield increases from the addition of NI
to spring-
applied
N
even though inhibitor persistence is limited
by high soil
temperatures. Overall, the probability of
corn yield response from currently available
NI in the
southeastern U.S. is poor for fall-applied N
and fairto
poor for spring-applied N.
Eastern
Cornbelt
The
response of corn to
NI
application
has
been
more consistent over years in the eastern Cornbelt
than other portions of the United States
because of
high rainfall, finer textured soils, and cold
soil
temperatures during the winter.
However, overall only
about 50 and
70
of the trials with spring- and fall-
applied N have shownyield response from NI. Yield
responses have been obtained with both spring- and
fall-applied
N in Indiana, Kentucky, Ohio, and
southern Illinois. The consistency of yield responses
to
NI
has been less in Michigan, Wisconsin, Missouri,
central and
northern Illinois, and
Iowa than
in
other
eastern Cornbelt states.
However, all states
in the
eastern
Cornbelt have studies showing
corn yield
increases from NI addition, and the largest and most
consistent increases are normally observed with fall-
applied
N or with non-tillage programs.
There
is a good probability of obtaining a yield
increase from application of NI to fall-applied
ammoniacal fertilizers
in the eastern Cornbelt
because of the large N
loss normally associated with
fall applications. The use of NI will allow producers to
apply N
fertilizers somewhat earlier than generally
consideredfeasible (50°Fis traditionally considered
the maximum
soil temperature for application of
ammoniacal fertilizers
in the fall without a
NI).
Fall
application of N is not recommended for low CEC
coarse-textured soils because of the possibility of
ammonium leaching.
The probability is good that NI added to spring-
preplant N will Increase yields of corn growth on fine-
textured soils of the eastern Cornbelt because of the
likelihood of N losses by denitrification after
fertilization. Only a fair probability exists for a yield
response to
NI added with spring-preplant N applied
to
silt
barns and coarser textured soils. The
probability of loss in such
soils depends upon
the
nitrification rate following fertilization, the internal
drainage ofthe soil, and the
distribution
and
intensity
Region
Time of
application
of studies with
yield Increase
yield
increase2
Southeast (GA,
MD. NC, SC, TN)
Fall
Spring
17
43
14
15
Eastern Cornbelt (IL,
IN, OH, KY)
Fall
Spring
Spring (no-till)
69
51
82
9
3
13
Northem
Cornbelt (MI, MN, WI)
not irrigated
FaIl
Spring
25
17
5
12
Western Cornbelt (KS, MN, NE)
irrigated coarse-textured
soils
Spring
52
30
Western Cornbelt (KS,
NE)
irrigated medium- and
fine-textured soils
Spring
10
5
Table
7. RegIonal Summary of Corn Yield Responses from Nitrification
Inhibitors Addedto Ammonlacal
Fertilizers Appled
at Varying Times.1
‘Datataken from a variety of research progress reports and published materials.
2Average Increases obtained
in
experiments where NI addition gave significant yield increases.
5

of rainfall. Heavy
rains occurring 2 to
8 weeks
after
fertilization may result in extensive
N
losses and yield
responses to NI application.
However, if a below
average rainfall
period follows fertilization, little N loss
or response to
NI will occur.
Western Cornbelt
Few yield responses
to
NI have been
observed
with dryland corn orirrigated
corn produced
on fine-
textured soils
in Minnesota, North Dakota,
South
Dakota,
and other states west of the Missouri river.
However, the use of NI
has resulted in increased
yields in areas
where preplant N
is
applied to irrigated
corn grown on
sandy soils. Data from
Minnesota
(Table
4) illustrate the type of responses that are
sometimes obtained when a
NI
is used to reduce
nitrate leaching in irrigated sandy soils.
There is
poor probability of yield response with
spring-appliedfertilizer for dryland corn production in
the western Cornbelt; however, with irrigated coarse-
textured
soils the probability ofa yield increase
improves. There is a fair probability of a response to
NI with fall applied fertilizer on finer textured soils. Fall
application of arnmoniacal fertilizers
is not
recommended for sandy soils.
ADDITIONAL CONSIDERATIONS WHEN
USING NITRIFICATION INHIBITORS
More consistent yield responses have been
obtained with no-till grown corn than
with conventional
tillage
systems fertilized in the spring
(Tables
3 and 8).
This finding
results from greater infiltration rates,
higherwater contents, a higher population of
denitrifying bacteria in no-till soils and, thus, increased
N
losses from
leaching and/or denitrification.
The
probability of yield responses
to NI
added to
spring-sidedress-applied N
Is considered low for all
soils
because the fertilizer is added close to the time
of plant uptake. However, a few investigators
in
the
eastern Cornbelt have observed significant yield
increasesfrom
NI
added to
early sidedressed N
fertilizers.Additional studies are needed at several
locations in all corn-growing regions to determine the
long-term probability of a response to NI application
with sidedress N
should exist
on coarse-textured soils
receiving excess
rainfall
or irrigation
water.
The
commercially available NI
have properties
that affect how they can be
addedto various types of
fertilizers. N-Serve and Dwell can
be impregnated
on
solid fertilizers, or an
emulsifiable formulation may be
mixed with N
solution fertilizers.
N-Serve can be
added directly to bulk anhydrous ammonia because of
its high
solubility in liquid ammonia. However,
Dwell is
not soluble in ammonia, butcan
be added to
anhydrous ammonia with a small electric pump that
meters the compound
into the ammonia stream
between the nitrolatorand the manifold system
on
the
applicator.
Soil texture
Application
time
Region of the U.S.
Eastern
Southeast
Cornbeit
Western
Cornbelt
—Probability of corn yield
increase’-—
Sands
Fall
Spring
Poor
Poor
Fair
Fair
Poor
Fair2
Loamy sands, sandy
barns, and loams
Fall
Spring
Poor
Fair
Fair
Fair3
Poor
Fair3
Silt barns
Fall
Poor
Good
Fair
Spring
.
Fair
Fair3
Poor
Clay loams and
clays
Fall
Spring
Poor
Good
Fair
Good
Fair
Poor
Reference to products in
this publication is not intended
to be
an endorsementto
the excius onoiotherswr,icn
using such
products assume responsibility for their use in accordance with
may be
similar. Persons
A publication of the National Corn Handbook Project
and justice for all
The
U.S. Department
ofAgriculture (USDA) prohibits discrimination
In all its
programs and activities on
the
basis of
race, color,
national origin, gender,
religion, age,
disability, political
beliefs,
sexual orientation, and marital or
family status. (Not all prohibited
bases
apply
to all programs.) Many materials
can be made available in alternativeformats forADA
clients. To file
a
complaint ofdiscrimination, write USDA. Office of civil Rights, Room 326-W,
Whitten 8ullding,
14th and
IndependenceAvenue, SW,
Washington,
oc
20250-9410or call
202-720.5984.
Issued In
furtherance
of Cooperative
Extension
work, Acts of
May
8 and June
30,
1914,
in cooperation
with
the
U.S. Department ofAgriculture.
Stanley
R.
Johnson, director, cooperative Extension Service, Iowa State University of
Science and Technology, Ames. Iowa.
File:
Agronomy2-2
Table
8. Probability of Corn Yield Increase from the Addition of NI to Ammoniacal Fertilizers Applied
at
Varying Times.
‘Poor
=
less than 20
chance of yield Increase
at any locatIon any year; fair
=
20.60
chance ofincrease; good
=
greater than 60
chance ofIncrease.
2
Fair for Irrigated soils, poor for dryland corn.
Good
for no-till production systems.

m
C-)

EXHIBIT C
SUMMARY
DOCUMENT OF EFFLUENT AMMONIA-NITROGEN
REDUCTION EVALUATIONS FOR NOVEON-HENRY
PLANT

BR OWN
AND
CALD
WELL

Back to top


MEMORANDUM
TO:
Mark Latham, Esq.
JOB NO:
27-21522.001
FROM:
T. Houston Flippin, P.E., DEE
DATE:
May 17, 2002
SUBJECT:
Ammonia-Nitrogen Treatment Alternatiyes
Support Exhibit
Brown
and
Caidwell
is
providing
below
a
summary
of
information
intended
to
support
the
discussion
of
ammonia-nitrogen
(NH3-N)
treatment
alternatives
described
in
the
Petition
For
Adjusted
Standard.
This
information is
the
product of treatability testing,
full-scale plant
testing,
and data provided by the
Noveon-Henry Plant staff.
In
order to develop treatment alternatives, a “design influent and effluent wasteload” was
required.
This
wasteloads were
developed based on individual wastestream data gathered in
1995 and effluent
data gathered in 1999 through
2000
and are
summarized
below in Tables I and 2.
A flow schematic
is provided in
Attachment A of the wastewater treatment
facility
(WWTF)
provided
at the
Henry
Plant.
Table
1.
InfluentWasteload Used In Developing Treatment Alternatives
Parameter
PVC Tank
PC Tank
C-18 Tank
Holding Pond!
Well No.3 Waters
Total
Flowrate, gpm
Average
401
107
6
46
560
Peak
499
150
15
105
769
SCOD, lbs/day
Average
2,650
8,280
1,320
50
12,300
Peak
4,330
10,840
2,940
50
18,160
Estimated BOD, lbs/day
Average
795
.
2,485
395
15
3,690
Peak
1,300
3,250
880
15
5,445
TKN,
lbs/day
Average
459
494
82
3
1038
Peak
640
693
198
7
1537
NH3-N, lbs/day
Average
295
62
27
1
385
Peak
411
87
66
3
571
P:\PROJ\21522\M051702
Latham.doc

Memorandum
to
MarkLatham, Esq.
May
17, 2002
Page 2
Table 2.
Effluent Wasteload Used In Developing Treatment Alternatives
Parameter
Effluent Value
NH3-N, lbs/day
Average
909
Peak
1408
The following treatment alternatives
were considered for ammonia reduction.
Illustrations of each
are
provided in Attachment A.
alkaline
air stripping of PC Tank contents with off-gas
collection and treatment (No.
I)
alkaline
air stripping of PVC Tank
contents
(No.
2)
alkaline
air stripping of secondary clarifier effluent (No. 3)
struvite
(NH4MgPO46FI2O) precipitation from combined influent (No.
4)
breakpoint chlorination of secondary clarifier effluent (No. 5)
nitrification of PVC Tank wastewater (non-PC wastewaters) (No. 6)
nitrification of combined wastewater (No. 7)
ion exchange treatment of final
effluent
(No. 8)
ozonation of
final effluent
(No.9)
nitrification of secondary clarifier effluent (tertiary nitrification)
(No. 10)
A
summary
of
conceptual
level
capital
costs
for
each
of
these
alternatives
are
summarized
in
Table 3.
The total costs presented in
this
table are considered accurate to within ±
30 percent.
Table
3.
Capital Cost Estimates For Treatment Alternatives
Upgrade Components
Upgrade Costs in
$
Millions for Treatment Alternative Number
1
2
3
4
5
6
7
8
9
10
Pretreatment
0.65
0.10
0.00
0.05
0.00
0.02
0.43
0.00
0.00
0.00
Primary Treatment
0.00
0.00
0.00
0.00
0.00
0.25
0.00
0.00
0.00
0.00
Secondary Treatment
0.00
0.00
0.00
0.00
0.00
1.12
1.91
0.00
0.00
0.00
Tertiary Treatment
4.21
0.75
0.57
4.6
4.00
Sub-total
0.65
0.10
4.21
0.05
0.75
1.39
2.34
0.57
4.6
4.00
Sitework/Interface Piping
0.10
0.01
0.32
0.01
0.11
0.21
0.35
0.09
0.20
0.50
Electrical/Instrumentation
0.25
0.16
0.40
0.16
0.26
0.36
0.50
0.24
0.50
0.30
Contractor Indirects (8
)
0.05
0.01
0.34
0.00
0.06
0.11
0.19
0.05
0.37
0.32
Engin./Constr. Mgmt (18 )
0.12
0.02
0.76
0.01
0.14
0.25
0.42
0.10
0.83
0.72
Performance Bonds (I
)
0.01
0.00
0.04
0.00
0.01
0.01
0.02
0.00
0.05
0.04
Sub-total
1.17
0.30
6.07
0.22
1.33
2.33
3.82
1.04
6.54
5.88
Contingency
(15 )
0.18
0.04
0.91
0.03
0.20
0.35
0.57
0.16
0.98
0.88
Total Installed Cost
1.35
0.34
6.98
0.25
1.53
2.68
4.40
1.20
7.52
6.76
l’:’PROJ\21522\M051702
Latham.doc

Memorandum to Mark Latham, Esq.
May
17, 2002
Page
3
A summary of conceptual level operations and maintenance costs for each of these alternatives are
summarized in
Table
4.
The
total costs presented
in
this
table
are considered
accurate
to
within
±
30 percent.
Table
4.
Annual Operating and
Maintenance Cost Estimates For Treatment Alternatives
Cost Components
Annual O/M Costs in
$ Thousands for
Treatment Alternative Number
1
2
3
4
5
6
7
8
9
10
Labor ($40/hour)
32
32
60
8
.
60
60
60
60
30
60
Electrical ($0.06/kwh)
64
29
214
0
4
10
98
10
1,363
88
Natural
Gas ($0.06/therm)
18
0
0
0
0
0
0
0
0
0
Chemicals (Plant Costs)
0
1,794
575
642
1,028
218
788
147
226
459
ResinReplace. ($35/cu ft)
0
0
0
0
0
0
0
242
0
0
Off-site Disposala
0
0
0
0
0
0
0
51
0
0
MaintenanceMaterials~’
17
2
105
1
19
11
45
14
115
22
Sub-total
130
1,858
954
652
1,111
299
990
524
1,735
629
Contingency
(10
)
13
186
95
65
111
30
99
.52
173
63
Total Annual
143
2,044
1,049
717
1,222
329
1,089
576
1,908’
692
a Cost of disposing of spent
regenerant containing
29.7
assumed to be $0.10/gallon.
b
Based on 5 percent of equipment costs.
percent
by
weight NH4C1
(8
percent N)
A
comparison
of alternatives
regarding present worth
costs and ammonia
removal is provided in
Table 5.
Table 5.
Comparison of Present Worth Costs and Ammonia Removal for Treatment Alternatives
.
Components
Treatment Alternative Number
1
2
3
4
5
6
7
8
9
10
NH3-NRemoval,lbs/day
247
147
864
217
891
423
891
891
891
891
NH3-N Removal,
27
16
95
24
98
47
98
98
98
98
Present Worth Costs
Capital
1.35
0.34
6.98
0.25
1.53
2.68
4.40
1.20
7.52
6.76
0/Ma
0.96
13.71
7.04
4.81
8.20.
2.20
7.31
3.87
12.80
4.64
Total
2.31
14.06
14.02
5.06
9.73
4.88
11.71
5.07
20.32
11.41
a
Based on 10 year period,
8 percent annual interest,
and no
salvage value.
P:\PROJ\2l522\M05t702 Latham.doc

BROWN
AND
CALD
WELL
Nashville, Tennessee
P:/PROJ/21522/~ig1
FIGURE
1
BLOCK FLOW
DIAGRAM
OF WASTESTREAM
SOURCES AND
WWTF

~
________
_____p~j~ren~j
~~u’.-Pc
Wastestreaj~—
~
PC
Tank
To Primary
Treatment
ALTERNATIVE NO.1
- ALKALINE AIR STRIPPING OF PC TANK CONTENTS
~~icSod*
2~’~
Defoamer
__—~~
Air
~furi~±~
PVC
Tank
To Primary
Treatment
ALTERNATIVE NO.2- ALKALINE AIR STRIPPING
OF PVC TANK CONTENTS
Off-Gas
~
Treatment
_____
Packed Tower
I
~
SulfuricA ~
ALTERNATIVE NO.3- ALKALINE AIR STRIPPING OF SECONDARY CLARIFIER EFFLUENT
I—
I
Existing Equipment
EJ
New
Equipment
FIGURE 2
BLOCK FLOW
DIAGRAM
OF ALKALINE
AIR STRIPPING
TREATMENT ALTERNATIVES
(Nos.
1, 2, and 3)
BROWN
AND
I
C
A
L
D
w
E
L
L
Nashville,
Tennessee
PJPROJ/21522/Fig

-It-
---
r
~-~---
-‘;
~
pH Adjustment
Coagulation
Sedimentation
To_Biotreater~
I
To FilterPj~’~
__
-‘
~icSod~-
NOTE:
Existing
FeCI3 Addition would be discontinued
-
Existing Equipment
E~J
New
Equipment
FIGURE 3
BLOCK FLOW
DIAGRAM
OF STRUVITE
PRECIPITATION TREATMENT ALTERNATIVE
-
(No.4)
BROWN
AND
(~
A
~
m
i~
i
i
Nashville,
Tennessee
PJPROJ/21522/F1g3
i-’
1/
YT
Li
Li
Li

Existing
Equipment
~
New
Equipment
FIGURE 4
BLOCK FLOW
DIAGRAM
OF BREAKPOINT
CHLORINATION
ALTERNATIVE
-
(No.5)
BROWN
AND
PJPROJ/215221F194
C
A
L
D
W
E
L
L
Nashville,
Tennessee

_____________
——
.
I
__________
~I
11.11
.
I
II.•.
~
Existing Equipment
New
Equipment
FIGURE 5
BLOCK FLOW
DIAGRAM OF NON-PC WASTESTREAM
NITRIFICATION TREATMENT ALTERNATIVE
ROWN
AND
(No.
6)
P:/PROJ/21522/Fig
ALD
WELL

~iI
-
--
-
----
I
~-
-
Existing Equipment
L.....J
New
Equipment
l\\\\\\’~ Upgraded Equipment
FIGURE 6
BLOCK FLOW
DIAGRAM OF COMBINED WASTESTREAM
NITRIFICATION TREATMENT ALTERNATIVE
(No. 7)
BROWN
AND
PJPROJ!215221Fig 6
CALD
WELL

Treatment
L—.~linoisRiver
V
-
I
I
Existing
Equipment
LT~1
New
Equipment
FIGURE 8
-
BLOCK FLOW
DIAGRAM
OF OZONE
TREATMENT ALTERNATIVE
-
(No.9)
-
BROWN
AND
C
A
L
D
~
B
L
L
Nashville,
Tennessee
P:/PROJ/21522iFig
8
-
________________

I
Existing
Equipment
£~J
New
Equipment
FIGURE 9
BLOCK FLOW
DIAGRAM
OF TERTIARY
NITRIFICATION TREATMENT ALTERNATIVE
(No. 10)
BROWN
AND
CALD
WELL
Nashville, Tennessee
P:/PROJ/21522JFig 9

m
:3-
C

EXHIBIT D
SUMMARY
OF COST
ANALYSIS
FOR PROVIDING INCREMENTAL
EFFLUENT AMMONIA-NITROGEN REMOVAL AT THE
NOVEON-HENRY
PLANT

WWTF Component
Basis
PC
Tank
PVC Tank
Effluent
Effluent
Effluent
Effluent
Effluent
Struvite
Effluent
BP
Non-PC
Combined
Stripping
Stripping
Stripping
Stripping
Stripping
Stripping
Stripping
Precipitation
Chlorination
Nitrification
Nitrification
W/
Off.gas
w!o Off-gas
W/
Off-gas
No
Off-gas
No Off.gas
No
Off-gas
No Off-gas
75
removal
50
removal
25
removal
Additional Operations!
Maintenance Labor
‘LaborHours
800
800
1500
1300
1300
1000
1000
200
1500
1500
1500
*
Annual Cost,
$
$40/hr
32000
32000
60000
52000
52000
40000
40000
8000
60000
60000
60000
Electrical
Usage
‘hp
162
75
545
505
450
300
300
1
10
25
250
kwh
1058664
490122
3561553
3300155
2940732
1960488
1960488
6535
65350
163374
1633740
*AnnuaICost,$
$0.06/kwh
63520
29407
213693
198009
176444
117629
117629
392
3921
9802
98024
Maintenance Materials
*
LowEnd Equipment
Costs,
$
330,000
40,000
2106000
1263600
1013600
631800
379080
15000
375000
222,000
890,000
AnnuaiCosts,$
5ofECosts
16500
2000
105300
63180
50680
31590
18954
750
18750
11100
44500
Chemical
Costs
*
50
NaOH,
$ year
$240/ton
0
1770431.04
434000
434000
434000
217000
108500
0
955541
217772
742484
98
H2S04, S/year
$46/ton
0
24238
141000
119850
119850
70500
35250
0
0
0
45333
*
75
H3PO4, S/year
$335/ton
0
0
0
0
0
0
0
407160
0
0
0
*
62
Mg(OH)2, S/year
$220/ton
0
0
0
0
0
0
0
235205
0
0
0
*
98
HCI, $Iyear
$70/ton
0
0
0
0
0
0
0
0
0
0
0
*
Chlorine Gas, S/year
$50/ton
0
0
0
0
0
0
0
0
72681
0
0
Annual Costs
s/year
0
1794669
575000
553850
553850
287500
143750
642365
1028222
217772
787817
Annual
ResIn
Replacement, S/year
$90/cu ft
0
0
0
0
0
0
0
0
0
0
0
Annual
Off-site
Disposal, S/year
$0.10/gal
Natural Gas Cost, $/
year
Annual
Cost, S/year
$0.06/therm
18240
0
0
0
0
0
0
0
0
0
0
SubtotalAnnual
Costs,
S/year
130260
1858076
953993
867039
832974
476719
320333
651507
1110893
298674
990341
Contingency (10),$/yr
13026
185808
95399
86704
83297
47672
32033
65151
111089
29867
99034
Total Annual
Cost, 5/year
143286
2043884
1049393
953743
916271
524391
352367
716657
1221982
328542
1089375
Present Worth of Annual
Costs
$
10 years
961448
13714462
7041424
6399617
6148181
3518665
2364380
4808771
8199501
2204516
7309707
8 percent interest
Capital Costs, $
1,345,138
344,023
6,983,076
4,522,426
3,770.418
2,453,930
1.541.358
253,748
1,526,625
2.676,729
4,397,370
Total Present Worth, $
2,306,586
14,058,484
14,024.500
10,922,043
9,918,598
5,972,595
3,905,738
5,062,519
9,726,126
4,881,245
11,707,077
Average
NH3-N Removal, lbs/day
247
147
864
864
648
432
216
217
891
423
891
Average NH3-N Removal,
27.2
16.2
95.0
95.0
71.3
47.5
23.8
23.9
98.0
46.5
98.0
Present Worth Cost,
$Jlb NH3-N
2.56
26.13
4.45
3.47
4.20
3.79
4.96
6.39
2.99
3.16
3.60

Additional
Operations!
Maintenance Labor
*
Labor Hours
*
Annual
Cost,
$
$40/hr
Electrical Usage
*hp
25
18.75
12.5
6.25
225
168.75
112.5
56.25
kwh
163374
122531
81687
40844
22727273
1470366
1102775
735183
367592
*
Annual Cost, $
$0.06/kwh
9802
7352
4901
2451
1363636
88222
66166
44111
22055
Maintenance Materials
*
LowEnd Equipment
Costs,
$
*
Annual Costs,
$
5
ofE Costs
Chemical Costs
*
50
NaOH,
$
year
$240/ton
*
98
H2SO4, S/year
$46/ton
*
75
H3P04, S/year
$335/ton
*
62
Mg(OH)2, $/year
$220/ton
*
98
HCI,
S/year
$70/ton
• Chlorine Gas, S/year
$50/ton
Annual Costs, S/year
Annual ResIn Replacement, S/year
$90/cu ft
Annual Off-site Disposal. s/year
$0.10/gal
Natural Gas Cost, 5! year
Annual Cost, s/year
$0.06/therm
Subtotal Annual Costs, S/year
Contingency (10),5/yr
Total Annual Cost, S/year
Present Worth ofAnnual Costs
5
10 years
8 percent interest
Capital Costs,
5
Total Present Worth,
$
Average NH3-N Removal, lbs/day
Average NH3-N Removal,
Present Worth Cost, $/lb NH3.N
WWTF Component
Basis
Effluent
Effluent
Effluent
Effluent
Ozonation
Tertiary
Tertiary
Tertiary
Tertiary
Ion
Exchange
Ion
Exchange
Ion
Exchange
Ion Exchange
Nitrification
Nitrification
Nitrification
Nitrification
75
removal
50
removal
25
removal
75
removal
50
removal
25
removal
1500
1500
1500
1500
750
1500
1500
1500
1500
60000
60000
60000
60000
30000
60000
60000
60000
60000
284000
227200
170400
85200
2300000
444000
355200
266400
133200
14200
11360
8520
4260
115000
22200
17760
13320
6660
129861
97396
64930
32465
226145
458660
343995
229330
114665
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
0
17044
12783
8522
4261
0
0
0
0
0
0
0
0
0
0
0
0
0
0
146905
110179
73453
36726
226145
458660
343995
229330
114665
242449
181837
121224
60612
0
0
0
0
0
50727
38045
25363
12682
0
0
0
0
0
0
0
0
0
524083
408772
293462
176731
1734781
629082
487921
346761
203380
52408
40877
29346
17673
173478
62908
48792
34676
20338
576492
449650
322808
194404
1908259
691990
536713
381437
223718
3868259
3017150
2166041
1304450
12804419
4643251
3601346
2559441
1501151
1,198,024
1.095.472
787,814
480,157
7,523,300
6,762,000
6,223,800
4,264,200
2,304,600
5,066,283
4,112,621
2,953,855
1,784,607 20,327,719
11,405,251
9,825,146
6,823,641
3,805,751
891
668
445
223
891
891
668
445
223
98.0
73.5
49.0
24.5
98.0
98.0
73.5
49.0
24.5
1.56
1.69
1.82
2.20
6.25
3.51
4.03
4.20
4.68

m
:3-
m

EXHIBIT E
SUMMARY
TABLE
COMPARING
COST, EFFLUENT AMMONIA-NITROGEN
REDUCTION PERCENTAGES, RELIABILITY,
AND
PROS
AND
CONS OF
ALTERNATIVE EFFLUENT AMMONIA-NITROGEN REDUCTION
PROCESSES FOR THE NOVEON-HENRY
PLANT

-
--
-I
Comparison of Costs and Removals of Effluent NH3-N Removal Processes
for theNoveon-Henry Wastewater Treatment Facility with 10-Year Project
Life
Annual
Operating
Process
Capital Cost
($
millions)
Cost
($
millions/year)
Present Worth Cost’
Effluent NH3-N Removal
(Average )
($
millions)
($/lb NH3-N removed)
PC Tank Strippingwith
1.35
0.130
2.21
2.45
27
Off-gas Control
1.31
0.125
2.15
4.60
14
PVC Tank Stripping
0.344
2.04
14.1
26.13
16
without
Off-gas Control
0.317
2.03
14.0
51.89
8
Effluent
Strippingwith
6.98
1.05
14.1
4.42
95
Off-gas Control
Effluent
Strippingwithout
4.52
0.894
10.5
3.34
95
Off-gas Control
3.77
0.850
9.5
3.83
75
2.45
0.483
5.7
3.44
50
1.54
0.332
3.8
4.59
25
Struvite
Precipitation
0.254
0.669
4.74
5.99
24
0.254
0.539
3.87
6.53
18
Effluent Breakpoint
1.53
1.22
9.73
2.99
98
Chlorination
P~\PROJ\23417
-
Noveon\Henry
-
002\Ezhibit
E.doc
Page 1
of 2

Comparison of Costs and Removals of EffluentNH3-N Removal Processes
for the Noveon-Henry Wastewater Treatment Facility with 10-Year Project
Life
Process
Capital Cost
($
millions)
Annual
Operating
Cost
($
millions/year)
Present Worth Cost
-
Effluent NH3-N Removal
(Average )
($
millions)
($/lb NH3-N removed)
Non-PC Nitrification
2.68
0.329
4.88
3.16
47
Combined Single-Stage
4.40
1.09
11.7
3.60
98
Nitrification
MBT Removal Process
0.86
0.441
3.82
Less Than 25
WWTF
Upgrades
3.54
0.649
7.88
0
EffluentIonExchange
1.20
1.10
0.79
0.48
0.688
0.533
0.379
0.222
5.82
4.67
3.33
1.97
1.79
1.88
2.01
2.38
98
75
50
25
Effluent Ozonation
7.52
1.91
20.3
6.25
98
TertiaryNitriflcation
6.76
6.22
4.26
2.30
0.692
0.536
0.381
0.223
11.4
9.83
6.82
3.81
3.51
4.03
4.20
4.68
98
75
50
25
ai
0 years at 8
interest.
P:\PROJ\23417
-
Noveon\Henty
-
002\Exhibit
E.doc
Page 2 of 2

Comparison of Costs and Removals of Effluent NH3-N Removal Processes
for the Noveon-Henry Wastewater Treatment Facility
with
20-Year Project
Life
Annual Operating
Process
Capital Cost
($
millions)
Cost
($
millions/year)
Present Worth
Costa
EffluentNH3-N Removal
(Average )
($
millions)
($/lb NH3-N removed)
PC Tank Strippingwith
1.35
0.130
2.63
1.46
27
Off-gas Control
1.31
0.125
2.54
2.72
14
PVC Tank Stripping
-
0.344
2.04
20.4
18.90
16
without Off-gas Control
0.317
2.03
20.2
37.43
8
Effluent Stripping with
6.98
1.05
17.3
2.71
95
Off-gas Control
Effluent Stripping without
4.52
0.894
13.3
2.12
95
Off-gas Control
-
3.77
0.850
12.1
2.44
75
2.45
0.483
7.2
2.17
50
1.54
0.332
4.8
2.90
25
Struvite
Precipitation
0.254
0.669
6.8
4.30
24
0.254
0.539
5.5
-
4.64
18
Effluent Breakpoint
1.53
1.22
13.5
1.08
98
Chlorination
-
P:\PROJ\23417
-
Noveon\Henry
-
0OZ\Exhibit E.doc
Page 1 of2

Comparison of Costs and Removals of Effluent NH3-N Removal Processes
for the Noveon-Henry Wastewater Treatment Facility with 20-Year Project
Life
Process
Capital
Cost
($
millions)
Annual
Operating
Cost
($
millions/year)
Present Worth Cost
Effluent NH3-N Removal
(Average
)
($
millions)
($/lbNH3-N removed)
Non-PC Nitrification
2.68
0.329
5.9
1.91
47
Combined Single-Stage
4.40
1.09
15.1
2.32
98
Nitrification
MBT
Removal Process
0.86
0.441
5.2
Less Than 25
WWTF
Upgrades
3.54
0.649
9.9
-
-
0
Effluent
IonExchange
1.20
1.10
0.79
0.48
0.688
0.533
0.379
0.222
8.0
6.3
4.5
2.7
1.23
1.27
1.36
1.63
98
75
50
25
EffluentOzonation
7.52
1.91
26.3
4.05
98
Tertiary Nitrification
.
6.76
6.22
4.26
2.30
0.692
0.536
0.381
0.223
13.6
11.5
8.0
4.5
2.09
2.36
2.46
2.76
98
75
50
25
years at 8
interest.
P:\PROJ\23417
-
Noveon\Henry
-
O02\Exhibi~
E.doc
Page 2
of 2

Comparison of Removals
and
Reliability of Effluent NH3-N Removal Processes
for theNoveon-Henry Wastewater Treatment Facility
Process
Effluent NH3-N Removal
Reliability
(Average
)
Rating1
Comments
PC Tank Strippingwith
27
8
Involves adding surface aerator, oversized withdrawal fan, off-gas collection
Off-gas Control
and thermal oxidation of off-gas. Off-gas collection and treatment are
needed
for VOC control. No chemical addition required since PC Tank
contents are
normally pH
11
s.u. Simple to operate. Performance will vary as volatile amine
content varies in wastewater. Average removals of 0 to 27 percent could be
achieved
by
varying
the
size ofthe surface aerator placed in the
tank.
PVCTank Stripping
16
7
Involves adding caustic addition
and
surface aerator toPVCtank contents.
without Off-gas Control
Acid additionin
primary
system will be required to lowerpH to 9.0 s.u. Simple
to operate. Strong foaming potential in PVCTank which would reduce
effectiveness. Performance will vary
based on production discharges ofNH3-N
and volatile amines, and NH3-N returned in sludge dewatering
filtrate and
tertiary filter backwash. Removals of 0 to
16 percent could be achieved by
varying the size of the surface aerator placed in the tank.
Wifi increase effluent
TDS.
Effluent
Stripping
with
95
7
Involves pumping sand filter effluent through two
packed
towers in series.
Off-gas Control
Caustic is added to increasepH to 11.5 s.u. and acid is added to lower the
treated effluentpH to 8 s.u. Off-gas is directed to an acid scrubber for recovery
of (NH4)2SO4. Scrubber discharge would be disposed
off-site. Complex to
operate. Equipmentmustbe housed in heated building to prevent freezing.
Fouling of tower mediawith precipitants is anticipated. Removals of
75
to
95
percent would be achieved
by treating the whole effluent through different
sized columns. Removals of 25 to 50 percent would be achieved by treating
only a portion
of the final
effluent.
Will
increase effluentTDS.
Page 1 of4

Comparison of Removals
and Reliability
of Effluent NH3-N Removal Processes
for the Noveon-Henry Wastewater Treatment Facility (Continued)
Process
Effluent NH3-N Removal
Reliability
(Average
)
Rating1
Comments
Effluent Stripping without
95
8
Same as above but without off-gas
collection and treatment.NH3-N would be
Off-gas
Control
discharged to atmosphere.
Will
increase effluentTDS.
Struvite Precipitation
24
6
Involves feedingmagnesium hydroxideand
phosphoric acid to
existingprimary
treatment system. Simple to operate. However,the precipitantis prone to foul
pumps
and
piping. Removal could be varied between 18
and
24 percent
dependingupon the quantity ofmagnesium hydroxide added. Performance will
vary strictlyas a functionofinfluentNH3-N load.
Will
increase effluentTDS.
Effluent Breakpoint
98
9
Involves routing secondary clarifier effluent through chlorinationstep prior to
Chlorination
tertiary
filtration. Causticis fed to maintainpH control. Reliable process.
Creates safety concernsandmayform chlorinated organics.
Will
increase
effluentTDS.
Non-PC Nitrification
47
-
7
Involves using existing activated sludge system to provideBOD removal
and
nitrification ofPVCwastewater. Treated effluent from
this
systemwould be
combined
with PC
wastewaterand treated
in
new activated sludge system.
Complex system to operate. Two WWTFs that would be subject to upset.
Performance would vary as a function of PVC NH3-N and
amine loading.
Will
increase
effluent
TDS.
Page 2 of 4
P:\PROJ\23417
-
Noveon\Henry
-
002\Table
Alternative NH3.doc

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